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From the 11/19/2021 release of VAERS data:

Found 2,686 cases where Vaccine is COVID19 and Symptom is Aborted pregnancy or Abortion or Abortion complete or Abortion early or Abortion incomplete or Abortion induced or Abortion late or Abortion missed or Abortion of ectopic pregnancy or Abortion spontaneous or Abortion spontaneous complete or Abortion spontaneous incomplete or Foetal cardiac arrest or Foetal death or Premature baby death or Premature delivery or Stillbirth

Government Disclaimer on use of this data



Case Details (Sorted by Onset Date)

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VAERS ID: 1634695 (history)  
Form: Version 2.0  
Age: 23.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-02-28
Onset:2021-03-01
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-08-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Malaise, Maternal exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: PVIUS2021001198

Write-up: Maternal exposure during pregnancy; unwell; Miscarriage; This spontaneous retrospective pregnancy case was reported by an other health care professional and describes the occurrence of ABORTION SPONTANEOUS (Miscarriage) in a 23-year-old female patient (gravida 1) who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 28-Feb-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On 01-Mar-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced ABORTION SPONTANEOUS (Miscarriage) (seriousness criteria hospitalization prolonged, medically significant and congenital anomaly). On an unknown date, the patient experienced MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy) and MALAISE (unwell). The delivery occurred on an unknown date, which was reported as Abortion NOS. For foetus 1, The outcome was reported as Spontaneous Abortion NOS. On 01-Mar-2021, ABORTION SPONTANEOUS (Miscarriage) had not resolved. At the time of the report, MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy) had resolved and MALAISE (unwell) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered ABORTION SPONTANEOUS (Miscarriage) to be related. No further causality assessments were provided for MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy) and MALAISE (unwell). It was reported that the patient was pregnant at the time she received the second dose, 1st trimester. This was her first pregnancy. Right after she was given the vaccine, she started feeling unwell, 2 days later, she miscarried her baby No information on concomitant medication were reported. No treatment details were reported. Company comment: This is a case of vaccine exposure during pregnancy with associated AEs of malaise and serious of event Spontaneous abortion for this 23 year old female after receiving the second dose of the vaccine.; Sender''s Comments: This is a case of vaccine exposure during pregnancy with associated AEs of malaise and serious of event Spontaneous abortion for this 23 year old female after receiving the second dose of the vaccine.


VAERS ID: 1653910 (history)  
Form: Version 2.0  
Age: 44.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2021-03-10
Onset:2021-03-01
Submitted: 0000-00-00
Entered: 2021-08-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Pregnancy test positive, Ultrasound scan, Uterine dilation and curettage
SMQs:, Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/a
Current Illness: N/a
Preexisting Conditions: POTS/Dysautonomia
Allergies: N/a
Diagnostic Lab Data: Positive pregnancy tests, ultrasounds, blood tests, d&c to remove what was left of the pregnancy.
CDC Split Type:

Write-up: A week after receiving the covid vaccine I ovulated a full week early and became unexpectedly pregnant on or about March 18, 2021. This pregnancy resulted in a miscarriage on April 29, 2021.


VAERS ID: 1661217 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: California  
Vaccinated:2021-03-24
Onset:2021-03-01
Submitted: 0000-00-00
Entered: 2021-09-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER2613 / 2 LA / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Bedridden, Blood test, Dizziness, Heavy menstrual bleeding, Malaise, Movement disorder, Nausea, Pregnancy test, Thrombosis, Ultrasound scan, Vaginal haemorrhage
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Anticholinergic syndrome (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Akathisia (broad), Dyskinesia (broad), Dystonia (broad), Parkinson-like events (broad), Thrombophlebitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: COVID-19; Hypertension; Obesity
Allergies:
Diagnostic Lab Data: Test Date: 2021; Test Name: blood tests; Result Unstructured Data: Test Result:Normal; Test Date: 202102; Test Name: Pregnancy test; Result Unstructured Data: Test Result:positive; Test Date: 2021; Test Name: ultrasound; Result Unstructured Data: Test Result:normal
CDC Split Type: USPFIZER INC202101085060

Write-up: heavy excessive vaginal bleeding; a lot of blood clots with her period; Miscarriage; Nausea; Dizziness / she feels dizzy; feeling sick; she couldn''t get out of bed; felt like she couldn''t walk; had her period longer than 3 weeks/had her period almost a month now; This is a spontaneous report from a contactable consumer or other non-healthcare professional (patient). This consumer reported information for both mother and fetus/baby. This is a maternal report. A 33-years-old pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot Number: ER2613; Expiration Date: Jul2021), dose 2 via an unspecified route of administration in left arm on 24Mar2021 (age at the time of vaccination was 33 years) as dose 2, single for covid-19 immunisation at Medical Clinic. The vaccine was not administered at Military Facility. The patients Medical History (including any illness at time of vaccination) was reported as hypertension and obesity from an unknown date and unknown if ongoing. It was reported that the patient has already previously had covid. The patient concomitant medications were reported as no. Previously the patient had received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot Number: EN6199; NDC unknown, Expiration Date: Jun2021), dose 1 via an unspecified route of administration on 03Mar2021 (age at the time of vaccination was 33 years) for covid-19 immunisation. It was reported that the time when the vaccination was given was in the morning. History of all previous immunization with the Pfizer vaccine considered as suspect and additional Vaccines Administered on Same Date of the Pfizer Suspect was reported as None. Prior vaccinations within 4 weeks and AE(s) following prior vaccinations were reported as none. On an unspecified date in 2021, the patient got the first vaccine and then ended up getting pregnant in february 2021, she couldn''t get out of bed, had her period longer than 3 weeks/had her period almost a month now and felt like she couldn''t walk. On 31Mar2021, the patient experienced a lot of blood clots with her period, miscarriage, dizziness / she feels dizzy and nausea. On an unspecified date in Mar2021, the patient was feeling sick. On an unspecified date in Aug2021, the patient experienced heavy excessive vaginal bleeding. The patient reported that the events has worsened. It was reported that the patient had been having side effects- extensive bleeding and a lot of blood clots with her period. She got the first vaccine and then ended up getting pregnant in February 2021. By March 2021 the patient had to take her second dose and when she did she had a miscarriage right after. The patient started feeling sick and went to the emergency room and they didnt know if it was from the miscarriage or not. The patient has had heavy excessive vaginal bleeding for a whole month. The patient called her primary care provider and when she went to the doctor she got a lot of tests done. The tests showed that the patient did not have a tube pregnancy when she went to the emergency room to make sure it was fine. The patient did an ultrasound and blood tests and it was normal, they just said it was a miscarriage. The patient was so sick with the side effects of the miscarriage. The patient had so much dizziness she could not get out of bed and felt like she could not walk. The patient reported, everything was moving, the patient was moving and everything was still and she feels dizzy. The patient has had her period longer than 3 weeks. The caller saw online that there were other people with long periods. The patients friend called her and said she has had a long period too. The patient was concerned because she has had her period almost a month now. At first the patient thought it was a normal long period after the miscarriage. It happened in March and then April and May was whatever. The miscarriage was not as even heavy as this month. The patients vaginal bleeding starts slowing down and then comes in heavy again. The patient had tests on her heart on 19Apr2021 to make sure everything was okay and it was normal, that was when she saw the cardiologist. Reportedly, on 30Mar2021 the patient went to her OB/GYN to see how the baby was doing and said they could not find the heartbeat. The patient went to the hospital a few days later to make sure things were okay, the patient thinks this was on 04Apr2021 or 05Apr2021. Reportedly, heavy excessive vaginal bleeding started this month(unspecified). After the miscarriage the patient went to doctor and they checked her tubes and uterus. Everything was fine and nothing was abnormal. When the patients period was longer than 3-4 weeks, the patient started thinking what was going on now. The patient realized she was pregnant in Feb2021 towards the end of the month, she had some blood work done and it said she was pregnant. The patient later clarified and confirmed that she received both doses of the vaccines in March. It was reported that, they used the camera to look inside her uterus. The patient had all of her medical records with all of the tests she had done and the results if Pfizer needs them. Reportedly the pregnancy test was done in Feb2021 and the result was positive. The patient later clarified and confirmed that she went to her OB/GYN on 31Mar2021 and that was when they could not find the babys heartbeat. Reportedly, the Adverse events required visit to emergency room/ physicians office. The mother reported she became pregnant while taking bnt162b2. On an unspecified date in 2021, the patient underwent lab tests and procedures which included blood test: normal and ultrasound scan: normal. On an unspecified date in Feb2021 the patient underwent lab tests and procedures which included pregnancy test: positive. The outcome of the events The caller got the first vaccine and then ended up getting pregnant in February 2021, a lot of blood clots with her period, miscarriage, heavy excessive vaginal bleeding, had her period longer than 3 weeks/had her period almost a month now, she couldn''t get out of bed, felt like she couldn''t walk and feeling sick was unknown. The outcome of the events nausea, Dizziness / she feels dizzy was not recovered. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1713680 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Georgia  
Vaccinated:2021-02-01
Onset:2021-03-01
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-09-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: No e
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: 6weeks after 2nd shot miscarriage


VAERS ID: 1716895 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Wisconsin  
Vaccinated:2020-12-23
Onset:2021-03-01
   Days after vaccination:68
Submitted: 0000-00-00
Entered: 2021-09-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0142 / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Fatigue, Headache, Human chorionic gonadotropin, Nausea, Pain
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: n/a
Current Illness: n/a
Preexisting Conditions: n/a
Allergies: n/a
Diagnostic Lab Data: POCT HCG 6/17/21
CDC Split Type:

Write-up: Headache, Severe Nausea, Body Aches, Fatigue @ 0800, Miscarraige at 4 weeks


VAERS ID: 1749395 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Maryland  
Vaccinated:2021-02-04
Onset:2021-03-01
   Days after vaccination:25
Submitted: 0000-00-00
Entered: 2021-09-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ1686 / 2 UN / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Human chorionic gonadotropin
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Confirmation of initial HCG level detecting pregnancy, followed by HCG level decline.
CDC Split Type:

Write-up: Miscarriage


VAERS ID: 1751736 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated:0000-00-00
Onset:2021-03-01
Submitted: 0000-00-00
Entered: 2021-10-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USJNJFOC20210955581

Write-up: This spontaneous pregnancy report received from a patient via social media concerned a female of unspecified age, race and ethnicity. The patient''s height, and weight were not reported. No past medical history or concurrent conditions were reported. It was not reported whether the patient had been pregnant before. The patient received Covid-19 vaccine ad26.cov2.s (suspension for injection and route of admin were not reported) dose was not reported, 1 total administered on MAR-2021 for prophylactic vaccination. The batch number was not reported. Per procedure, no follow-up will be requested for this case. No concomitant medications were reported. On MAR-2021, the patient had vaccine exposure during pregnancy. The date of the patient''s last menstrual period and expected delivery were not reported. On an unspecified date, the patient had miscarriage. Patient reported that she had seen many people who had the vaccine and had miscarriage. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the miscarriage and vaccine exposure during pregnancy was not reported. This report was serious (Other Medically Important Condition).; Sender''s Comments: V0: 20210955581-COVID-19 VACCINE AD26.COV2.S-miscarriage. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s) 20210955581-COVID-19 VACCINE AD26.COV2.S-vaccine exposure during pregnancy . This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS


VAERS ID: 1121421 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-01
Onset:2021-03-01
   Days after vaccination:59
Submitted: 0000-00-00
Entered: 2021-03-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Miscarriage (Previous)
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021244218

Write-up: Miscarriage of pregnancy; This is a spontaneous report from a contactable physician. This is a report received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-TPP46117099C2221787YC1614601322189, Safety Report Unique Identifier GB-MHRA-ADR 24868877. A 35-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: not reported) via an unspecified route of administration in Jan2021 at 30 ug (0.3ml), single for COVID-19 vaccination. Medical history included previous miscarriage. Concomitant medications were not reported. The patient experienced miscarriage of pregnancy on 01Mar2021. The event was reported as medically significant. The clinical course was reported as follows: Patient had routine COVID vaccination at start of January 2021. Fell pregnant after this and then suffered a miscarriage at 5 or 6 weeks after the vaccination. Has previously miscarried and this may be unrelated. The outcome of the event of miscarriage of pregnancy was recovered on 01Mar2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Sender''s Comments: In agreement with reporter, event miscarriage of pregnancy is likely an intercurrent condition and unrelated to BNT162B2 based on available information. The patient had previous miscarried history.


VAERS ID: 1179107 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-14
Onset:2021-03-01
   Days after vaccination:46
Submitted: 0000-00-00
Entered: 2021-04-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ZE8492 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure during pregnancy, SARS-CoV-2 test, Ultrasound scan vagina, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Folic acid supplementation; Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Date: 20210319; Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test; Test Date: 20210322; Test Name: TV US; Result Unstructured Data: Test Result:unknown results
CDC Split Type: GBPFIZER INC2021319599

Write-up: Early miscarriage; vaginal bleeding; Maternal exposure during pregnancy/ exposed to the medicine first-trimester (1-12 weeks).; This is a spontaneous report from a contactable physician received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202103220904099680 and Safety Report Unique GB-MHRA-ADR 24995519. A 35-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 14Jan2021 (Lot Number: ZE8492) as single dose, second dose received via an unspecified route of administration on 18Mar2021 (Lot Number: ER1749) as single dose for COVID-19 immunisation. Medical history included pregnancy, patient no longer pregnant at the time of reporting and vitamin supplementation. 1 previous physiologic pregnancy. Patient has not had symptoms associated with COVID-19 Patient is not enrolled in clinical trial. Patient was pregnant at time of vaccination, not currently breastfeeding. Patient last menstrual period date on 11Jan2021. Concomitant medication included folic acid (unknown manufacturer) taken for folic acid supplementation. The patient experienced early miscarriage, vaginal bleeding in Mar2021, maternal exposure during pregnancy/ exposed to the medicine first-trimester (1-12 weeks) from an unknown date in 2021. Patient had vaginal bleeding within 48 hours from injection of second dose of Pfizer and miscarriage. The patient underwent lab tests and procedures which included COVID-19 test: negative on 19Mar2021. Patient has not tested positive for COVID-19 since having the vaccine. TV US done 22Mar2021 with unknown results. The outcome of the events early miscarriage and vaginal bleeding was recovering. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1199751 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2018-01-18
Onset:2021-03-01
   Days after vaccination:1138
Submitted: 0000-00-00
Entered: 2021-04-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / UNK - / -
UNK: VACCINE NOT SPECIFIED (NO BRAND NAME) / UNKNOWN MANUFACTURER TU01D1D / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Cervix haematoma uterine, Drug ineffective, Embedded device, Hysterometry, Investigation, Microbiology test, Pregnancy with contraceptive device, Ultrasound scan, Venous thrombosis in pregnancy
SMQs:, Lack of efficacy/effect (narrow), Haemorrhage terms (excl laboratory terms) (narrow), Embolic and thrombotic events, venous (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Overweight; Postpartum state (no periods)
Preexisting Conditions: Medical History/Concurrent Conditions: Elective abortion (1, due to fetal Trisomy 21); Multigravida (3); Parity 1 (spontaneous); Spontaneous abortion (1)
Allergies:
Diagnostic Lab Data: Test Date: 20180118; Test Name: Hysterometry; Result Unstructured Data: Test Result:8-9; Test Date: 202103; Test Name: Investigation; Result Unstructured Data: Test Result:Lower leg thrombosis; Test Date: 202103; Test Name: Microbiology test; Result Unstructured Data: Test Result:Unremarkable; Test Date: 20180215; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:IUS in situ; Test Date: 20180626; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:IUS in situ; Test Date: 20181127; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:IUS in situ; Test Date: 20191007; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:IUS in situ; Test Date: 20201006; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:IUS in situ; Test Date: 20210302; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:diagnosis of early pregnancy, 6+4; Mirena in situ; Comments: At position control diagnosis of early pregnancy, 6+4 weeks; Mirena in situ, cervical, mural, not removed; Test Date: 20210303; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:cervical hematoma requiring cervical dilation
CDC Split Type: DEPFIZER INC2021342342

Write-up: lack of drug effect; Cervical hematoma; Mirena in situ, cervical, mural, not removed; Early pregnancy (6+4 weeks); Lower leg thrombosis in last week of pregnancy; Spontaneous abortion at week 8+3; This is a spontaneous report from a non-contactable physician downloaded from the Medicines Agency (MA) -WEB, company number DE-BAYER-2021-093273. A 41-years-old female patient received unspecified dose bnt162b2 (COMIRNATY, (Batch/Lot Number: Unknown), via an unspecified route of administration on an unspecified date as for covid-19 immunisation. levonorgestrel (MIRENA), intra-uterine from 18Jan2018 (Batch/Lot Number: TU01D1D) to an unspecified date, at 20 ug, daily continuously for contraception. Medical history included multigravida, abortion induced from Sep2016 to an unknown date 1, due to fetal Trisomy 21 , ongoing postpartum state no periods , abortion spontaneous , primiparous from Mar2015 to an unknown date spontaneous , ongoing overweight. The patient''s concomitant medications were not reported. on 03Mar2021 The patient experienced spontaneous abortion at week 8+3 (abortion spontaneous), cervical hematoma (cervix haematoma uterine), lower leg thrombosis in last week of pregnancy (venous thrombosis in pregnancy), mirena in situ, cervical, mural, not removed (embedded device) (medically significant) on 02Mar2021, early pregnancy (6+4 weeks) (pregnancy with contraceptive device), lack of drug effect (drug ineffective). The patient underwent lab tests and procedures which included hysterometry: 8-9 on 18Jan2018, investigation: lower leg thrombosis on Mar2021, microbiology test: unremarkable on Mar2021, ultrasound scan: ius in situ on 15Feb2018, ultrasound scan: ius in situ on 26Jun2018, ultrasound scan: ius in situ on 27Nov2018 , ultrasound scan: ius in situ on 07Oct2019, ultrasound scan: ius in situ on 06Oct2020, ultrasound scan: diagnosis of early pregnancy, 6+4; mirena in situ on 02Mar2021 At position control diagnosis of early pregnancy, 6+4 weeks; Mirena in situ, cervical, mural, not removed , ultrasound scan: cervical hematoma requiring cervical dilation on 03Mar2021.The outcome of the events was recovered. No follow-up attempts needed, follow-up automatically provided by EMA.


VAERS ID: 1260080 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-01
Onset:2021-03-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ0553 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Investigation, SARS-CoV-2 test
SMQs:, Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CYCLOGEST; EVOREL; FOLIC ACID; FYBOGEL; PREGNACARE ORIGINAL [ASCORBIC ACID;BETACAROTENE;BIOTIN;CALCIUM PANTOTHENATE;COLECALCIFEROL;COPPER;CY; PROGYNOVA [ESTRADIOL VALERATE]
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Constipation; Folic acid supplementation; Lactation decreased; Miscarriage; Pregnancy (previous pregnancies reported was otherwise healthy, no issues)
Allergies:
Diagnostic Lab Data: Test Date: 20210301; Test Name: scan; Result Unstructured Data: Test Result:CRL 10mm and heartbeat; Test Date: 20210331; Test Name: scan; Result Unstructured Data: Test Result:no heartbeat and a CRL of 8.2mm; Test Date: 20210127; Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021394032

Write-up: Miscarriage of pregnancy; This is a spontaneous report from a contactable consumer (patient), received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-WEBCOVID-202104080915329640, Safety Report Unique Identifier GB-MHRA-ADR 25110243. A 38-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 01Mar2021 (Lot Number: EJ0553) as single dose for COVID-19 immunisation. Medical history included suppressed lactation, miscarriage, pregnancy, details of previous pregnancies reported was otherwise healthy, no issues. (patient no longer pregnant at the time of reporting), folic acid supplementation, and constipation. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. Concomitant medications included progesterone (CYCLOGEST) taken for pregnancy from 14Jan2021 to 31Mar2021; estradiol (EVOREL) taken for pregnancy from 14Jan2021 to 31Mar2021; folic acid (FOLIC ACID) taken for folic supplementation, start and stop date were not reported; plantago ovata (FYBOGEL) taken for constipation from 20Mar2021 to an unspecified stop date; ascorbic acid, betacarotene, biotin, calcium pantothenate, colecalciferol, copper, cyanocobalamin, folic acid, iodine, iron, magnesium, nicotinamide, phytomenadione, pyridoxine hydrochloride, riboflavin, selenium, thiamine mononitrate, tocopheryl acid succinate, zinc (PREGNACARE ORIGINAL) taken for pregnancy from 01Jan2021 to an unspecified stop date; estradiol valerate (PROGYNOVA) taken for pregnancy from 04Jan2021 to 31Mar2021. The patient experienced miscarriage of pregnancy in Mar2021. The mother reported she became pregnant while taking BNT162B2. The mother was 7 Weeks pregnant at the onset of the event. Patient had healthy scan at 7w+3 which showed CRL 10mm and heartbeat on 01Mar2021. She then had Pfizer 2nd dose on 04Mar2021. Her subsequent scan on 31Mar2021 showed no heartbeat and a CRL of 8.2mm. The fact that the CRL had shrunk implies the embryo died soon after the 8 week scan. Although this may be entirely unrelated to the Pfizer vaccine that she had, she thought she should report this for data gathering purposes. Patient has not tested positive for COVID-19 since having the vaccine. Unsure if the medicine have an adverse effect on any aspect of the pregnancy. Patient was exposed to the medicine first-trimester (1-12 weeks). Patient had an IVF pregnancy with an early scan at 7w+3 on 01Mar2021. There was a heartbeat and the CRL was 10mm (normal). Then had the Pfizer vaccine 2nd dose 3 days later on 04Mar2021. Her next scan on 31Mar2021 showed a missed miscarriage, CRL 8.2mm. The patient underwent lab tests and procedures which included investigation: crl 10mm and heartbeat on 01Mar2021, investigation: no heartbeat and a crl of 8.2mm on 31Mar2021, sars-cov-2 test: negative on 27Jan2021 No - Negative COVID-19 test. The outcome of the event was recovering. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1287182 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-04
Onset:2021-03-01
Submitted: 0000-00-00
Entered: 2021-05-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EP2166 / 2 RA / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Asthma; Migraine
Allergies:
Diagnostic Lab Data:
CDC Split Type: FRPFIZER INC2021435908

Write-up: Miscarriage; This is a spontaneous report from a contactable physician downloaded from a Regulatory Authority FR-AFSSAPS-NT20211090, Safety Report Unique Identifier FR-AFSSAPS-2021038423. A 29-year-old female patient received bnt162b2 (COMIRNATY), dose 2 intramuscular, administered in Arm Right on 04Mar2021 (Batch/Lot Number: EP2166) as a single dose for covid-19 immunisation. Medical history included migraine and asthma from an unknown date and unknown if ongoing. Date of last menstruation: 08Feb2021. The patient''s concomitant medications were not reported. It was reported that between 15 and 21Mar2021, the patient experienced spontaneous miscarriage (discovery on ultrasound of pregnancy dating stopped on 07Apr2021, with a gap of 3.5 weeks between dating measured 5 week of amenorrhea and expected 8 week of amenorrhea + 2 days). On 11Apr2021, spontaneous expulsion of the embryo was performed. The outcome of the event was recovered with sequelae. No follow-up attempts are possible, no information is expected.


VAERS ID: 1356368 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-20
Onset:2021-03-01
   Days after vaccination:9
Submitted: 0000-00-00
Entered: 2021-05-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Heavy menstrual bleeding, Maternal exposure during breast feeding, SARS-CoV-2 test
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Neonatal exposures via breast milk (narrow), Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: SPRINTEC
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Breast feeding
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative
CDC Split Type: GBMODERNATX, INC.MOD20211

Write-up: Miscarriage; Maternal exposure during breast feeding; Heavy periods; This regulatory authority case was reported by an other health care professional and describes the occurrence of ABORTION SPONTANEOUS (Miscarriage) in a 37-year-old female patient who received mRNA-1273 (Moderna CoviD-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included Breast feeding. Concomitant products included ETHINYLESTRADIOL, NORGESTIMATE (SPRINTEC) for Oral contraception. On 20-Feb-2021, the patient received second dose of mRNA-1273 (Moderna CoviD-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna CoviD-19 Vaccine) (Intramuscular) 1 dosage form. In March 2021, the patient experienced HEAVY MENSTRUAL BLEEDING (Heavy periods). On an unknown date, the patient experienced ABORTION SPONTANEOUS (Miscarriage) (seriousness criterion medically significant) and MATERNAL EXPOSURE DURING BREAST FEEDING (Maternal exposure during breast feeding). In March 2021, HEAVY MENSTRUAL BLEEDING (Heavy periods) had resolved. At the time of the report, ABORTION SPONTANEOUS (Miscarriage) and MATERNAL EXPOSURE DURING BREAST FEEDING (Maternal exposure during breast feeding) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: negative Negative. For mRNA-1273 (Moderna CoviD-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient had two heavy periods following the second dose. They happened more often than usual (every two weeks). Patient had not tested positive for COVID-19 since having the vaccine. Action taken with mRNA-1273 (Moderna COVID-19 Vaccine) in response to the event was not applicable. No illness, no medication at that time, apart from contraceptives (Sprintec). Patient had not had symptoms associated with COVID-19.Patient was not enrolled in clinical trial. Patient was not pregnant. Company comment: Limited information regarding the events has been provided at this time and is insufficient for causality assessment.; Sender''s Comments: Limited information regarding the events has been provided at this time and is insufficient for causality assessment.


VAERS ID: 1533200 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-21
Onset:2021-03-01
   Days after vaccination:39
Submitted: 0000-00-00
Entered: 2021-08-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0379 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Off label use, Product use issue, SARS-CoV-2 test
SMQs:, Termination of pregnancy and risk of abortion (narrow), Medication errors (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID; VITAMIN D [COLECALCIFEROL]
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Folic acid supplementation; Lactation decreased; Miscarriage; Pregnancy (Patient no longer pregnant at the time of reporting.); Pregnancy
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC202100950161

Write-up: Maternal exposure during pregnancy; Maternal exposure during pregnancy; Miscarriage; This is a spontaneous report from a contactable consumer or other non hcp received from The regulatory authority report number is GB-MHRA-WEBCOVID-202107251904488590-QZRKK. A 33-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL0379) via an unspecified route of administration on 21Jan2021 as DOSE 1, SINGLE (Age of vaccination: Unknown) for covid-19 immunization. Medical history included suppressed lactation, abortion spontaneous, pregnancy, pregnancy as Patient no longer pregnant at the time of reporting, vitamin supplementation. Concomitant medication(s) included folic acid (FOLIC ACID) taken for pregnancy, vitamin supplementation from 01Oct2020; cholecalciferol (VITAMIN D [COLECALCIFEROL]) taken for pregnancy from 01Oct2020. Patient has not had symptoms associated with COVID-19 Patient is not currently breastfeeding. Patient has not tested positive for COVID-19 since having the vaccine. Patient is not enrolled in clinical trial. Unsure the medicine have an adverse effect on any aspect of the pregnancy. Patient was exposed to the medicine first-trimester (1-12 weeks). On an unspecified date the patient experienced maternal exposure during pregnancy. On 01Mar2021 the patient experienced miscarriage. Missed miscarriage noted at 12 week scan, after experience spotting during the previous week. Advised the foetus had died between 6-7 weeks gestation. Had the pfizer vaccine a few days before conceiving the pregnancy. Unsure whether it is related or not, but had been advised by GP to not have my second dose of the vaccine until after my 1st trimester because of unknown risks. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on No - Negative COVID-19 test. The outcome of all event was unknown. Details of previous pregnancies: Previous successful pregnancy of MCDA twins. Conceived the failed pregnancy within days of having the pfizer vaccine. Details of scans or investigations: Missed miscarriage detected at 12 week scan. Foetus died at 6 weeks. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1085314 (history)  
Form: Version 2.0  
Age: 46.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-02-23
Onset:2021-03-02
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-03-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 013M20A / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Heavy menstrual bleeding, Menstruation irregular, Pregnancy test negative
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Over the Counter Probiotics, prescribed Vitamin D, Iron (not taken daily), Yaz (generic) Birth Control Pills and I get allergy shots every 7-14 days
Current Illness: None
Preexisting Conditions: Poly Cystic Ovarian Syndrome, seasonal allergies, migraines
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Exactly a week after the vaccine shot, I started a very heavy menstural period. It was not time yet. I am on birth control pills and I am very regular. It''s been a week and I am still on a heavy period. It was so bad that I purchased a pregnancy test because I was having a miscarriage. Test was negative.


VAERS ID: 1109162 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-01-28
Onset:2021-03-02
   Days after vaccination:33
Submitted: 0000-00-00
Entered: 2021-03-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK9231 / 2 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Human chorionic gonadotropin, Ultrasound scan, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Cellulitis in arm from Pneumovax
Other Medications: Prenatal vitamin Nasacort nasal spray Pantoprazole Tylenol prn
Current Illness:
Preexisting Conditions: Asthma, gerd
Allergies: Latex, penicillin, poppy seeds
Diagnostic Lab Data: Received 1st vaccine on January 7. Confirmed pregnant at facility on January 26. Received 2nd vaccine on January 28 (4w4d pregnant). Began bleeding on March 2. First ultrasound at Clinic when seen for bleeding (on March 7) measured gestational sac at 6w4d, was 10w at the time. HCG levels at 13,200. Seen at Clinic on March 8, HCG levels at 9,000. Passed gestional sac on March 11/12. Ultrasound done on March 15 showed no gestational sac.
CDC Split Type:

Write-up: Miscarriage of baby due on 10/3/21.


VAERS ID: 1111992 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Maine  
Vaccinated:2021-02-27
Onset:2021-03-02
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-03-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011A21A / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Premature delivery, Premature labour
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Pre-natal vitamins
Current Illness:
Preexisting Conditions:
Allergies: Penicillin
Diagnostic Lab Data:
CDC Split Type: vsafe

Write-up: I went into labor 03-02-2021 at 2:00am. I delivered my baby at 6:47am. I was 30 weeks pregnant at the time of delivery and my baby is in NICU. At this time baby is doing fine.


VAERS ID: 1124086 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: New York  
Vaccinated:2021-02-26
Onset:2021-03-02
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-03-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Cardiac arrest, SARS-CoV-2 test
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Acute central respiratory depression (broad), Cardiomyopathy (broad), Termination of pregnancy and risk of abortion (narrow), Respiratory failure (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210304; Test Name: Covid PCR test; Result Unstructured Data: Test Result:Pending
CDC Split Type: USPFIZER INC2021240019

Write-up: Miscarriage; Heart stopped on pregnancy; This is a spontaneous report from a contactable consumer (patient). A 42-year-old female patient received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date were not reported), via an unspecified route of administration in the left arm on 26Feb2021 06:00 PM at a single dose for COVID-19 immunisation. The patient''s medical history was not reported. The patient had no known allergies. The patient was 8 weeks pregnant at the onset of the event. Last menstrual date was on 01Jan2021. There were no concomitant medications in two weeks and no other vaccine in four weeks. The patient previously received her first dose of BNT162B2 on an unspecified date at 06:00 PM in the left arm for COVID-19 immunisation. The patient had not been diagnosed with COVID prior to vaccination. The patient experienced miscarriage and heart stopped on pregnancy on 02Mar2021 03:00 PM. Treatment was unknown. Event resulted in doctor or other healthcare professional office/clinic visit. The patient was due to deliver on an unknown date. The patient underwent Covid PCR test post vaccination on 04Mar2021, pending results. Outcome of the events was unknown. Information on lot/ batch has been requested.


VAERS ID: 1412869 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Oregon  
Vaccinated:2021-01-20
Onset:2021-03-02
   Days after vaccination:41
Submitted: 0000-00-00
Entered: 2021-06-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011L20A / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Human chorionic gonadotropin decreased, Ultrasound scan
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Declining HCG levels were drawn and ultrasound performed.
CDC Split Type:

Write-up: SAB/Miscarriage at 9 weeks gestation on 3/2/2021. Was 3 weeks pregnant on date of vaccine 1/20/2021, was unknown to be pregnant at the time. Had spontaneous miscarriage 6 weeks later. Have had prior uncomplicated pregnancy and delivery in 2018. No history of pregnancy loss/infertility.


VAERS ID: 1170670 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-01
Onset:2021-03-02
   Days after vaccination:60
Submitted: 0000-00-00
Entered: 2021-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH NOT KNOWN / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure during pregnancy, SARS-CoV-2 test
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? Yes
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness: Pregnancy (Patient no longer pregnant at the time of reporting.)
Preexisting Conditions: Medical History/Concurrent Conditions: Abortion (One pregnancy at 12 weeks which was aborted when I was very young.)
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021306634

Write-up: Maternal exposure during pregnancy/Patient was exposed to the medicine first-trimester (1-12 weeks); Pregnancy loss/Miscarriage; This is a spontaneous report from the regulatory authority report number is GB-MHRA-WEBCOVID-202103181901588430, Safety Report Unique Identifier: GB-MHRA-ADR 24972388. A contactable consumer reported that a 34-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH, COVID-19 VACCINE) via an unspecified route of administration, on an unspecified date in Jan2021 (lot number and expiry date: unknown), at a single dose, for COVID-19 immunisation. Medical history included pregnancy, which no longer exists at the time of reporting, and an abortion (one pregnancy at 12 weeks which was aborted when she was very young). The patient had no health issues, fit and healthy, non-drinker and non-smoker. Patient has not had symptoms associated with COVID-19, not enrolled in clinical trial, and not currently breastfeeding. Concomitant medication included folic acid taken for vitamin supplementation. The patient experienced maternal exposure during pregnancy. Patient was exposed to the medicine first-trimester (1-12 weeks). On 02Mar2021, the patient experienced pregnancy loss/miscarriage. Baby was very much wanted and planned after 16 years. The patient was advised to stay at home and let miscarriage take its course and only visit hospital if in severe pain or excessive bleeding. It was not reported if fetal autopsy was performed. The events were considered serious due to disability, other medically important condition and congenital anomaly. The patient underwent lab tests and procedures which included COVID-19 virus test: no - negative on an unspecified date. Outcome of the event pregnancy loss/miscarriage was recovered. Patient has not tested positive for COVID-19 since having the vaccine. The reporter''s causality assessment was not provided. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1087557 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Tennessee  
Vaccinated:2021-01-02
Onset:2021-03-03
   Days after vaccination:60
Submitted: 0000-00-00
Entered: 2021-03-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3246 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage following COVID vaccine.


VAERS ID: 1113620 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-07
Onset:2021-03-03
   Days after vaccination:24
Submitted: 0000-00-00
Entered: 2021-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Chills, Exposure during pregnancy, Fatigue, Muscle spasms, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Dystonia (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Ultrasounds on March 3 and 12. May still ultrasound again March 19 although I am bleeding today consistently.
CDC Split Type:

Write-up: I was trying for a pregnancy and was likely pregnant but not detectable at vaccine number 1. Found out about pregnancy a week or so before vaccine 2. (I was likely about 5 weeks pregnant then based on LMP of dec 22 with avg cycles of 35 days. Decided to get vaccine due to general advice that it is okay during pregnancy. (No known adverse effects). After dose 2, had about 10-12 hours of chills without fever and general fatigue. Shortly afterwards experienced mild cramps. This is my 5th pregnancy and I have no history of complications of any sort. Cramps are not usual for my pregnancies but I know it can be normal so I did not think anything of it. Mild spotting occurred but again did not think anything of it as I know it can be normal. I was scheduled for a first OB visit Mar 3 where I should have been 10 weeks. (Initial positive pregnancy test was Jan 29). Ultrasound showed empty 5.6 week gestational sac with a yolk sac and subchorionic hemorrhage. OB suspected pregnancy failure. We followed pregnancy with ultrasound of better quality 10 days later which showed a possible fetal pole and yolk sac but no heart beat and gestational sac measured at 6.0 weeks. Today March 18 awaiting repeat ultrasound tomorrow but started bleeding and cramping. Consistent with the start of the miscarriage. With no histories of abnormal pregnancies and with the gestational sac consistently measure at 6 weeks (matching to about the time of shot#2), I am inclined to believe that the second covid shot stopped the progression of my pregnancy. I am a huge pro vaccine health care provider but would recommend now an investigation into first trimester covid vaccinations and possibly not recommend this during that time period.


VAERS ID: 1261506 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Indiana  
Vaccinated:2021-03-03
Onset:2021-03-03
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011J20A / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnancy test (Negative home pregnancy test.)
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20210

Write-up: Miscarriage; Patient was unaware that she was pregnant; This spontaneous case was reported by a nurse and describes the occurrence of ABORTION SPONTANEOUS (Miscarriage) in a 30-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 011J20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included Pregnancy test (Negative home pregnancy test.) on 02-Mar-2021. On 03-Mar-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Mar-2021, the patient experienced EXPOSURE DURING PREGNANCY (Patient was unaware that she was pregnant). On 19-Mar-2021, the patient experienced ABORTION SPONTANEOUS (Miscarriage) (seriousness criterion medically significant). At the time of the report, ABORTION SPONTANEOUS (Miscarriage) and EXPOSURE DURING PREGNANCY (Patient was unaware that she was pregnant) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route), the reporter did not provide any causality assessments. No treatment or concomitant mediation were reported.


VAERS ID: 1284748 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: New York  
Vaccinated:2021-02-23
Onset:2021-03-03
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-05-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM9810 / 1 LA / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Cervical incompetence
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021427602

Write-up: Cervical insufficiency in pregnancy resulting in loss of pregnancy; Cervical insufficiency in pregnancy resulting in loss of pregnancy; This is a spontaneous report from a contactable healthcare professional (patient). A 31-year-old female patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EM9810) at the age of 31-years-old, via an unspecified route of administration in left arm on 23Feb2021 at 08:15 at single dose for COVID-19 immunization. The patient''s medical history and concomitant medications were reported as none. She has no COVID prior to vaccination, no other vaccines in four weeks, and no other medications in two weeks. The patient was pregnant. Her last menstrual date was on 11Oct2020. Her delivery date is on 18Jul2021. The patient received her COVID-19 vaccine in a hospital. She experienced cervical insufficiency in pregnancy resulting in loss of pregnancy on 03Mar2021 at 15:00. The events resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care, and hospitalization from 2021 to 2021 for 1 day. There was no treatment given in response to the events. She was not tested got COVID post vaccination. She received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN6205) at the age of 31-years-old, via an unspecified route of administration in right arm on 16Mar2021 at single dose for COVID-19 immunization. The outcome of the events was unknown.; Sender''s Comments: The information available is limited. The etiology for the reported events could be multifactorial in nature. However until more information is available the contributory role of the suspect product BNT162B2 cannot be completely ruled out based on the potential temporal association noted. This case will be updated when more information is available.The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1152129 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-16
Onset:2021-03-03
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-03-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, SARS-CoV-2 test
SMQs:, Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID; SERTRALINE
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Anxiety; Lactation decreased; Miscarriage; Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021290130

Write-up: Miscarriage of pregnancy/miscarriage; This is a spontaneous report from the regulatory authority. The regulatory authority report number is GB-MHRA-WEBCOVID-202103141805472760; Safety Report Unique Identifier GB-MHRA-ADR 24938529. A contactable consumer reported that a 23-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: unknown) via an unspecified route of administration, on 16Feb2021, at a single dose, for COVID-19 immunisation. Medical history included abortion spontaneous, lactation decreased, anxiety and pregnancy (patient was no longer pregnant at the time of reporting). Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. Concomitant medications included folic acid for vitamin supplementation, and sertraline from 05Dec2019 for anxiety. Patient was exposed to the vaccine before pregnancy. It was unsure if the vaccine had an adverse effect on any aspect of the pregnancy. The patient underwent scans or investigations on 03Mar2021, which showed miscarriage (miscarriage of pregnancy). Patient showed a negative COVID-19 virus test on an unspecified date. Outcome of the event was unknown. Patient has not tested positive for COVID-19 since having the vaccine. No follow up attempts are possible, information about lot/batch number cannot be obtained.


VAERS ID: 1074788 (history)  
Form: Version 2.0  
Age: 24.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-02-01
Onset:2021-03-04
   Days after vaccination:31
Submitted: 0000-00-00
Entered: 2021-03-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal death, Foetal heart rate abnormal, Placental disorder, Ultrasound antenatal screen abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: no
Current Illness: no
Preexisting Conditions: no
Allergies: no
Diagnostic Lab Data:
CDC Split Type:

Write-up: At 8 weeks pregnancy (2 weeks after first shot) started bleeding and had a subchorionic hematoma. By 10 week subchorionic hematoma resolved. Received second shot and of Feb. 1 week later, at 12 weeks pregnancy , fetus had no heart beat! It measured normal size (as expected) and limited normal first trimester anatomy by ultrasound. But NO heart beat. Something insulted this placenta to lead to fetal demise.


VAERS ID: 1081203 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Tennessee  
Vaccinated:2021-02-04
Onset:2021-03-04
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-03-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / -

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound uterus abnormal
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Azelastine nasal spray, benadryl, Prenatal vitamins, Breo Ellipts, Zyrtec, Pristiq
Current Illness: Asthma, Anxiety
Preexisting Conditions: Asthma, Anxiety
Allergies: Cats, Grass Pollen, Mold, Oak trees
Diagnostic Lab Data: Ultrasound confirmed spontaneous abortion
CDC Split Type:

Write-up: Patient had LMP on 1/12/21, so was most likely early pregnant at the time of her first vaccine. She then experienced a miscarriage on 3/1/21. She was assessed in the ER and then in our OBGYN office.


VAERS ID: 1106446 (history)  
Form: Version 2.0  
Age: 22.0  
Sex: Female  
Location: Kentucky  
Vaccinated:2021-02-27
Onset:2021-03-04
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-03-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6198 / UNK LA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal death, Full blood count normal, Laboratory test normal, Live birth, Pathology test, Postpartum haemorrhage, Premature labour
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Smarty Pants Prenatal Vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: CBC- normal within range for labor and delivery, normal also for postpartum hemorrhage and blood loss 3/6/21 and 3/7/21
CDC Split Type:

Write-up: 20 weeks and 3 days pregnant with a girl at time of COVID vaccine, due date July 14th 2021. Anatomy scan on 2/26/21 and everything was normal. Two prior pregnancies both healthy and carried full term in 2017 and 2019. Spontaneous preterm labor on March 6th, 2021. Resulted in baby being born and dying about an hour and a half later due to how early she was. Labs came back normal, no signs of infection, placenta pathology came back normal. Baby was healthy as of 2/26/21 and was born alive.


VAERS ID: 1124428 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Arizona  
Vaccinated:2021-02-25
Onset:2021-03-04
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-03-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9264 / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Menstruation irregular
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: No previous history of miscarriages. Miscarriage began 4 weeks after first covid vaccine dose. Est. Date of birth October 2021 Unusual menstrual cycles following miscarriage. Unsure if there is any relation.


VAERS ID: 1178242 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Illinois  
Vaccinated:2021-03-04
Onset:2021-03-04
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 010A21A / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion of ectopic pregnancy, Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Subfertility (Treated since 2018)
Preexisting Conditions: Medical History/Concurrent Conditions: Hypospadias; Pregnancy (one)
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20210

Write-up: This spontaneous retrospective pregnancy case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of ABORTION OF ECTOPIC PREGNANCY (Miscarriage) in a 31-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 010A21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included Hypospadias on 15-Jun-2019 and Pregnancy (one). Concurrent medical conditions included Subfertility (Treated since 2018). On 04-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. The patient''s last menstrual period was on 22-Jan-2021 and the estimated date of delivery was 29-Oct-2021. On 04-Mar-2021, the patient experienced EXPOSURE DURING PREGNANCY (pregnancy). On 05-Mar-2021, the patient experienced ABORTION OF ECTOPIC PREGNANCY (Miscarriage) (seriousness criterion medically significant). The patient received mRNA-1273 (Moderna COVID-19 Vaccine) beginning around the fifth week of the pregnancy. The delivery occurred on an unknown date. For neonate 1, The outcome was reported as Ectopic pregnancy. On 04-Mar-2021, EXPOSURE DURING PREGNANCY (pregnancy) had resolved. At the time of the report, ABORTION OF ECTOPIC PREGNANCY (Miscarriage) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. This is a case of product exposure during pregnancy with abortion ectopic pregnancy for this 31-year-old female. Patient will continue to be contacted for further monitoring of AEs post abortion.; Sender''s Comments: This is a case of product exposure during pregnancy with abortion ectopic pregnancy for this 31-year-old female. Patient will continue to be contacted for further monitoring of AEs post abortion.


VAERS ID: 1191412 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: South Carolina  
Vaccinated:2021-02-12
Onset:2021-03-04
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-04-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9266 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6205 / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Ultrasound scan
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin, progesterone suppository
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: 3/11, ultrasound
CDC Split Type:

Write-up: Pregnancy began January 13th. 4 weeks pregnant at first vaccine. 7 weeks pregnant at second vaccine. Miscarriage occurred in the week following the second vaccine. Exact date that the heartbeat stopped is not able to be determined but there was a heartbeat 3/3. I got the vaccine 3/4.


VAERS ID: 1120216 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-21
Onset:2021-03-04
   Days after vaccination:11
Submitted: 0000-00-00
Entered: 2021-03-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK4244 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Haemorrhage, SARS-CoV-2 test
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness: Pregnancy (Patient no longer pregnant at the time of reporting.)
Preexisting Conditions: Medical History/Concurrent Conditions: Gravida II; Lactation decreased; Parity 2
Allergies:
Diagnostic Lab Data: Test Date: 20210115; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:Yes - Positive COVID-19 test
CDC Split Type: GBPFIZER INC2021245920

Write-up: bleeding; Miscarriage; This is a spontaneous report from a contactable other health professional. This is a report received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-WEBCOVID-202103042111113750, Safety Report Unique Identifier GB-MHRA-ADR 24878583. A 26-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Solution for injection) dose 1 via an unspecified route of administration on 21Feb2021 (Batch/Lot Number: EK4244) at a single for covid-19 immunization. Medical history included decreased lactation, ongoing pregnancy however patient no longer pregnant at the time of reporting. Patient was pregnant at the time of vaccination. Patient last menstrual period was on 11Jan2021. There were no other meds/ vaccinations in past 3 months. Patient has not had symptoms associated with COVID-19, not enrolled in clinical trial and is not currently breastfeeding. Patient had 2 previous, successful & healthy pregnancies. Concomitant medications included folic acid taken for folic acid supplementation, start and stop date were not reported. The patient experienced bleeding on 04Mar2021 with outcome of unknown and miscarriage on 04Mar2021 with outcome of not recovered. The mother reported she became pregnant while taking bnt162b2. The mother was 6 weeks pregnant at the onset of the event. The mother was due to deliver on 18Oct2021. Additional information as described was, bleeding began 04Mar2021 and believe that miscarriage was side effect of vaccine. Patient had positive test after vaccine. Approx. 7 weeks 3 days pregnant at time of miscarriage. Patient was exposed to the medicine first-trimester (1-12 weeks). The patient underwent lab test included COVID-19 virus test: yes - positive covid-19 test on 15Jan2021. Patient has not tested positive for COVID-19 since having the vaccine No follow-up attempts are possible. No further information expected.


VAERS ID: 1158628 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-20
Onset:2021-03-04
   Days after vaccination:43
Submitted: 0000-00-00
Entered: 2021-04-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6795 / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLPFIZER INC2021297557

Write-up: Missed abortion; This is a spontaneous report from a contactable other hcp downloaded from the Medicines Agency (MA) regulatory authority-WEB, regulatory authority number NL-LRB-00471378. A 30-year-old female patient received bnt162b2 (COMIRNATY), via an unspecified route of administration on 20Jan2021 (Batch/Lot Number: EJ6795) as SINGLE DOSE for covid-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient had her first vaccination at gestational age 3 weeks. Afterwards she found out she was pregnant and did not have the second vaccination. The missed abortion was diagnosed at approximately gestational age 9 weeks on 04Mar2021. The mother reported she became pregnant while taking bnt162b2. The mother was 3 Weeks pregnant at the onset of the event. The outcome of the event was not recovered. Sender''s comment: Since the nature of the reported reaction does imply seriousness according to one of the CIOMS critera, the reaction was considered as serious by the Centre Lareb. 15Mar2021 Follow-up received: Yes, this is correct. Between the first and second vaccinations she found out she was pregnant. That''s why she didn''t get the second vaccination. No follow-up attempts possible. No further information expected.; Reporter''s Comments: Text: BioNTech / Pfizer vaccine (Comirnaty): Past drug therapy BioNTech / Pfizer vaccine (Comirnaty): Missed abortion: Additional information ADR: Missed abortion detected at 4-3 confounding factors: COVID-19 vaccine exposure during pregnancy week: 3 COVID19: Previous COVID-19 infection: No. 15Mar2021 Follow-up received: Yes, this is correct. Between the first and second vaccinations she found out she was pregnant. That''s why she didn''t get the second vaccination.


VAERS ID: 1200035 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-07
Onset:2021-03-04
   Days after vaccination:25
Submitted: 0000-00-00
Entered: 2021-04-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH NOT KNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure during pregnancy, Scan
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness: Pregnancy (Patient no longer pregnant at the time of reporting.)
Preexisting Conditions: Medical History/Concurrent Conditions: Clinical trial participant (vaccine trial); Neural tube defect (Prevention of neural tube defect in pregnancy.); Pregnancy (First pregnancy)
Allergies:
Diagnostic Lab Data: Test Name: Scan; Result Unstructured Data: Test Result:at six weeks gestation showed foetal heartbeat
CDC Split Type: GBPFIZER INC2021342593

Write-up: Maternal exposure during pregnancy; Miscarriage; This is a spontaneous report from a contactable physician. This is a report downloaded from the regulatory authority. Regulatory authority report number GB-MHRA-WEBCOVID-202103221921316910, Safety Report Unique Identifier GB-MHRA-ADR 25001051. This physician reported information for both mother and fetus. This is the maternal report. Both cases are reported by regulatory authority as serious. This physician reported information for both mother and fetus. This is the maternal report. Both cases are reported by regulatory authority as serious. A 21-years-old female patient received BNT162B2 (COMIRNATY, formulation: Solution for injection, lot number: unknown), via an unspecified route of administration on 07Feb2021 at single dose for COVID-19 immunisation. Medical history included clinical trial participant in vaccine trial, first pregnancy from an unspecified date and there was prevention of neural tube defect in pregnancy. Patient was no longer pregnant at the time of reporting. Concomitant medications included folic acid at as dose of 400 microgram taken for vitamin supplementation. It was reported that patient has not had symptoms associated with COVID-19, did not have a COVID-19 test, and is not currently breastfeeding. The patient experienced maternal exposure during pregnancy on an unspecified date with outcome of unknown, foetal heartbeat on an unspecified date with outcome of unknown, miscarriage on 04Mar2021 with outcome of recovered. The patient underwent lab tests and procedures on an unspecified date, which included private scan at six weeks of gestation which showed foetal heartbeat. The outcome of the event maternal exposure during pregnancy was unknown and for miscarriage was recovered. The clinical assessment: First pregnancy. Patient was exposed to the medicine first-trimester (1-12 weeks). Details of scans or investigations: Private scan at six weeks gestation showed foetal heartbeat. The reporter assessment of the causal relationship of the events with the suspect product was not provided at the time of this report. Since no determination has been received, the case is managed based on the company causality assessment. No follow-up attempts are possible. No further information is expected. Information about lot/batch number cannot be obtained.


VAERS ID: 1265288 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-25
Onset:2021-03-04
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-04-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Miscarriage; Pregnancy (Patient no longer pregnant at the time of reporting.); Vitamin supplementation
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021405379

Write-up: Maternal exposure during pregnancy; Miscarriage of pregnancy/miscarriage; This is a spontaneous report from a contactable consumer. This is a report received from the Regulatory Agency. Regulatory authority report number GB-MHRA-WEBCOVID- 202104122334044390, Safety Report Unique Identifier GB-MHRA-ADR 25129099. A 39-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration on 25Feb2021 as single dose for COVID-19 immunisation. Medical history included abortion spontaneous, pregnancy (patient no longer pregnant at the time of reporting) and vitamin supplementation. Unsure if patient has had symptoms associated with COVID-19 Not had a COVID-19 test. Patient is not enrolled in clinical trial. Patient was not currently breastfeeding. Since the vaccination, the patient had not tested positive for COVID-19. Concomitant medication included folic acid taken for vitamin supplementation. On an unspecified date, maternal exposure during pregnancy and on 04Mar2021, miscarriage of pregnancy/miscarriage. It was also reported as, the miscarriage was probably unrelated to Pfizer but I am reporting just in case it is useful data. I miscarried at 5 weeks. Had vaccination day 27 of cycle and didn''t know I had conceived. It was unsure that, the medicine have an adverse effect on any aspect of the pregnancy. Patient was exposed to the medicine first-trimester (1-12 weeks). The outcome of the event miscarriage of pregnancy was recovered on 09Mar2021 (as reported) and other event was unknown.


VAERS ID: 1438612 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-04
Onset:2021-03-04
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER1741 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Gynaecological examination, Maternal exposure during pregnancy, Scan, Ultrasound scan vagina
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Asthmatic; Folic acid supplementation; Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Name: Internal examinations; Result Unstructured Data: Test Result:Unknown; Test Name: scan; Result Unstructured Data: Test Result:Unknown; Test Name: vaginal scan; Result Unstructured Data: Test Result:Unknown; Comments: 2 x vaginal scan
CDC Split Type: GBPFIZER INC2021710250

Write-up: Miscarriage; Maternal exposure during pregnancy/; This is a spontaneous report from a contactable consumer. This is a report received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202106141859133570-BSAME, Safety Report Unique Identifier GB-MHRA-ADR 25472785. A 32-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 04Mar2021 (Lot Number: ER1741), as dose 2, single for COVID-19 immunisation. Historical vaccine was taken for first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 26Jan2021 (Lot Number: EK4243) as single dose for COVID-19 immunisation. Medical history included an asthmatic patient, pregnancy, patient no longer pregnant at the time of reporting, and folic acid supplementation. Concomitant medication included folic acid taken for vitamin supplementation. The patient experienced maternal exposure during pregnancy on 04Mar2021 and on 03May2021, patient had miscarriage considered a disability and caused hospitalization. However patient believed she conceived around 8 days after having had the second dose of the vaccine (cannot be confirmed). Patient reported that this was her first pregnancy. Scan showed that the fetus stopped developing at 6 weeks when it should have been roughly 8 weeks. Relevant investigations or tests conducted: internal examinations, 2 x scan and 2 x vaginal scan. Followed by surgical management for the incomplete miscarriage. Patient was exposed to the medicine before pregnancy. Patient has not tested positive for COVID-19 since having the vaccine. The patient recovered with sequelae from the event miscarriage on 18May2021. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1524300 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-22
Onset:2021-03-04
   Days after vaccination:41
Submitted: 0000-00-00
Entered: 2021-08-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EMO477 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Scan
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: Scan; Result Unstructured Data: Test Result:no heart beat; Comments: Scan confirmed no heart beat.
CDC Split Type: IEPFIZER INC202100927104

Write-up: Miscarriage (missed); This is a spontaneous report from a contactable other hcp downloaded from the regulatory authority-WEB, regulatory authority number. Safety Report Unique Identifier. A 37-year-old female patient received bnt162b2 (COMIRNATY, solution for injection, Lot Number: EMO477), dose 1 via an unspecified route of administration on 22Jan2021 as dose 1, single for covid-19 immunisation. The patient''s medical history and concomitant medications were not reported. On 04Mar2021, the patient went for an early pregnancy scan and no heartbeat was detected, the foetus was measuring 6+3/40 instead of 8+2/40. The patient reported that she found out that she was pregnant on 08Feb.The patient reported that the potential for a miscarriage was predicted and another scan was booked for two weeks later. The second scan confirmed there was no heartbeat. The outcome of the event was recovered on an unknown date in 2021. No follow-up attempts are needed. No further information is expected.


VAERS ID: 1211156 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-06
Onset:2021-03-05
   Days after vaccination:58
Submitted: 0000-00-00
Entered: 2021-04-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0142 / 1 LA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL8982 / 2 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion induced, Exposure during pregnancy, Foetal renal impairment, Prenatal screening test abnormal, Renal dysplasia
SMQs:, Acute renal failure (narrow), Congenital, familial and genetic disorders (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lexapro, nature made prenatal vitamins, honest prenatal DHA
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: March 5th, fetal scan by perinatologist
CDC Split Type:

Write-up: Fetal renal anomaly, bilateral MCDK resulting in pregnancy termination at 21 weeks. Delivery date was estimated on July 15


VAERS ID: 1218811 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-02-10
Onset:2021-03-05
   Days after vaccination:23
Submitted: 0000-00-00
Entered: 2021-04-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9269 / 1 UN / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6198 / 2 UN / IM

Administered by: Private       Purchased by: ?
Symptoms: Amniocentesis normal, Foetal death, Foetal gastrointestinal tract imaging abnormal, Foetal hypokinesia, Inappropriate schedule of product administration, Single umbilical artery, Stillbirth, Ultrasound antenatal screen abnormal, Viral test negative
SMQs:, Congenital, familial and genetic disorders (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Medication errors (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: None.
Preexisting Conditions: ADHD. All meds discontinued before pregnancy.
Allergies: Nkda, no food allergies or other allergies.
Diagnostic Lab Data: can be provided Utrasounds, labwork
CDC Split Type:

Write-up: is 38 yo healthy G5P 2012 at time of event. -LMP 10/14/2020, EDC 7/21/2021 -Prenatal Ultrasound on 1/15/2021, size consistent with GA, 13 2/7 days, 3 vessel cord, rest WNL -received first Pfizer Covid-19 vaccine 2/10/2021 at 16 0/7 GA -received second Pfizer Covid-19 vaccine 3/1/2021 (19 days from first, NOT recommended 21 DAYS) -3/12/2021 had MFM level II ultrasound for advanced maternal age. -3/12/21 US revealed early IUGR est. fetal weight 296gm, GA consistent with 19/37 GA, now SINGLE uterine artery and echogenic bowel -Amnio, NITP, TORCH all normal/neg -4/3//21 mother noted no movements, fetal demise confirmed, delivered stillborn 4/4/21


VAERS ID: 1531771 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-03-02
Onset:2021-03-05
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-08-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6205 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Haemorrhage, Inappropriate schedule of product administration, Laboratory test abnormal, Placental infarction, Premature labour, Premature separation of placenta, Stillbirth, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Medication errors (narrow)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: None
Preexisting Conditions: Chronic hypertension
Allergies: None
Diagnostic Lab Data: 5/4/2021: Placenta tissue exam confirming a placental infarct compromising less than 5% of the placental parenchyma
CDC Split Type:

Write-up: I received my first Pfizer vaccine on 12/22/2020 (Lot: EJ1685) unknowing that I was less than 2 weeks pregnant. I received my second Pfizer vaccine on 3/2/2021 when I was 13 weeks gestation. I developed bright red vaginal bleeding on 3/5/2021 and was later diagnosed with chronic placenta abruption due to an infarction in the placenta. Due to the chronic bleeding from the placenta abruption, I went into preterm labor at 21 weeks 5 days gestation. I unfortunately hemorrhaged and delivered my stillborn son on 5/1/2021 at 22 weeks 1 day gestation. I have recovered from the hemorrhage without known long term side effects.


VAERS ID: 1859245 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Tennessee  
Vaccinated:2021-02-01
Onset:2021-03-05
   Days after vaccination:32
Submitted: 0000-00-00
Entered: 2021-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9261 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN9581 / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Haemorrhage, Pregnancy test urine positive, Ultrasound scan vagina
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zoloft 50 mg PNV Magnesium 400 mg Micronized Progesterone 50 mg
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Prolonged bleeding. Appt with DOCTOR 3/17/2021. Negative contents of conception at ultrasound 3/17/2021
CDC Split Type:

Write-up: G5P3 at the time. One second trimester loss 2015 placental abruption. No history of early miscarriages. LMP 1/29/2021 Positive urine pregnancy 2/26/2021. Miscarriage/bleeding 3/5/2021. Negative urine pregnancy 3/8/2021


VAERS ID: 1143193 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-29
Onset:2021-03-05
   Days after vaccination:35
Submitted: 0000-00-00
Entered: 2021-03-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH E10739 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness: Pregnancy
Preexisting Conditions: Medical History/Concurrent Conditions: Miscarriage
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021275797

Write-up: Miscarriage of pregnancy/Maternal exposure during pregnancy; The is a spontaneous report from a contactable other healthcare professional. This is a report received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-WEBCOVID-202103130951198060, Safety Report Unique Identifier GB-MHRA-ADR 24932804. A 42-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration on 29Jan2021 (Batch/Lot Number: E10739) as single dose for COVID-19 immunisation. Medical history included miscarriage and ongoing pregnancy. Patient has not had symptoms associated with COVID-19 and not had a COVID-19 test. Patient is not enrolled in clinical trial. Concomitant medication included folic acid taken for folic acid supplementation. The patient experienced miscarriage of pregnancy/maternal exposure during pregnancy (medically significant) on 05Mar2021 with outcome of recovered on 09Mar2021. The patient was no longer pregnant at the time of reporting. The patient became pregnant while taking bnt162b2. Last menstrual period date was 10Jan2021. The mother was 7 weeks pregnant at the onset of the event. The mother was due to deliver on 17Oct2021. Patient has not tested positive for COVID-19 since having the vaccine. The clinical course was reported as follows: Did the medicine have an adverse effect on any aspect of the pregnancy: Unsure. Patient was exposed to the medicine first-trimester (1-12 weeks). No follow-up attempts are possible. No further information is expected.


VAERS ID: 1250166 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2020-12-14
Onset:2021-03-05
   Days after vaccination:81
Submitted: 0000-00-00
Entered: 2021-04-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Scan
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Bleeding; Clotting disorder; Lactation decreased; Miscarriage
Allergies:
Diagnostic Lab Data: Test Name: Scan; Result Unstructured Data: Test Result:no heart beat; Comments: no heart beat; stopped developing at 7 weeks
CDC Split Type: GBPFIZER INC2021393680

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer, received from the Regulatory Authority. Regulatory authority report number GB-MHRA-WEBCOVID-202104081427582620, Safety Report Unique Identifier GB-MHRA-ADR 25113636. A 36-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date were not reported), via an unspecified route of administration on 14Dec2020 at single dose for COVID-19 immunisation. Medical history included lactation decreased, bleeding, multiple large clots, miscarriage (also reported no history of miscarriage). Patient has not had symptoms associated with COVID-19. Not had a COVID-19 test. Patient is not enrolled in clinical trial. Patient is not pregnant. Patient is not currently breastfeeding. The patient''s concomitant medications were not reported. The patient experienced miscarriage on 05Mar2021. The event was reported as serious (hospitalization). It was reported that vaccine was given on 14Dec2020, first day of last period was 20Dec2020. Miscarriage started 05Mar2021, scan showed no heart beat and stopped developing at 7 weeks. May or may not be related to covid vaccine. Patient has not tested positive for COVID-19 since having the vaccine. The patient was recovering from miscarriage. No follow-up attempts are possible. Information about batch number cannot be obtained.


VAERS ID: 1445364 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-24
Onset:2021-03-05
   Days after vaccination:9
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion, Maternal exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: JPPFIZER INC2021512990

Write-up: Abortion; the partner became pregnant; GENERAL INVESTIGATION TARGETING THE VACCINES (HEALTH CARE PROVIDERS HCPS) WHO ARE VACCINATED IN EARLY POST-APPROVAL PHASE (FOLLOW-UP STUDY) This is a report from a Non-Interventional Study source for Protocol C4591006 received from a contactable physician, study investigator. A 29-year-old male subject received the first and second dose of BNT162b2 (COMIRNATY, lot number and expiration date were not reported) via intramuscular at 0.3 mL single for COVID-19 immunization on 24Feb2021 and 17Mar2021 respectively. Medical history including family history was not reported. The subject did not receive any concomitant medication. The subject was not administered drugs (OTC drug or prescription drug) during the partner was pregnant. The partner of subject became pregnant. The date of last period of the partner was 21Mar2021. (pending clarification). The estimated date of pregnancy of the partner was 05Mar2021. (pending clarification). The period of pregnancy at the time of initial exposure was 1 week. The pregnancy of the partner of the subject became abortion. The event, abortion was classified as serious (medically significant). The partner did not smoke during this pregnancy. The partner did not drink alcohol during this pregnancy. The partner did not use illegal drugs during this pregnancy. The partner had no history of visiting the obstetrics department. The subject did not smoke while his partner was pregnant. The subject did not drink alcohol while his partner was pregnant. The subject did not use illegal drugs while his partner was pregnant. The reporter''s assessment of the causal relationship of the events with the suspect product was not provided at the time of this report. Since no determination has been received, the case is managed based on the company causality assessment. Information on the batch number has been requested.; Sender''s Comments: A contributory role of BNT162B2 to reported event cannot be fully excluded. However, the information provided is very limited and does not allow for a complete medical assessment. Case will be reassessed if additional information is received. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1141203 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Ohio  
Vaccinated:2020-12-29
Onset:2021-03-06
   Days after vaccination:67
Submitted: 0000-00-00
Entered: 2021-03-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 AR / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 AR / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Anembryonic gestation, Chills, Exposure during pregnancy, Fatigue, Pain, Ultrasound antenatal screen abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin, vitamin D
Current Illness:
Preexisting Conditions:
Allergies: Nkda
Diagnostic Lab Data: Ultrasound showing blighted ovum
CDC Split Type:

Write-up: Moderna COVID?19 Vaccine EUA Received 1st vaccine Dec 29, 2020, received 2nd vaccine while unknowingly pregnant on January 27, 2021. Had chills, fatigue, body aches night of 2nd vaccination. Found out pregnant Feb 7, 2021 at 4 weeks pregnant. Had blighted ovum/anembryonic pregnancy with miscarriage March 12, 2021.


VAERS ID: 1143201 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-18
Onset:2021-03-06
   Days after vaccination:16
Submitted: 0000-00-00
Entered: 2021-03-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL7834 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, SARS-CoV-2 test
SMQs:, Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Lactation decreased; Miscarriage; Multiparous (Details of previous pregnancies: para4 gravida 3)
Allergies:
Diagnostic Lab Data: Test Date: 20210123; Test Name: COVID-19 virus test; Test Result: Negative
CDC Split Type: GBPFIZER INC2021275957

Write-up: Miscarriage; This is a spontaneous report received from a contactable physician from the Regulatory Agency (RA). The regulatory authority report number is GB-GB-GB-MHRA-WEBCOVID-202103131547321580, Safety Report Unique Identifier GB-MHRA-ADR 24934898. A 42-year-old pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL7834) via an unspecified route of administration on 18Feb2021 at single dose for covid-19 immunisation. Medical history included miscarriage and lactation decreased. In addition, the patient had a twins 18 months old and one older child (Details of previous pregnancies: para4 gravida 3). Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. Concomitant medication included folic acid taken for folic acid supplementation. Patient has not tested positive for COVID-19 since having the vaccine. The patient experienced miscarriage on 06Mar2021. The patient had vaccine at approximately 7+6 weeks on 18Feb2021. Patient was exposed to the medicine first-trimester (1-12 weeks). She attended a private scan on 06Mar2021 and was told missed abortion on 8+6 weeks. The patient had surgical management of miscarriage. It is not known whether vaccine was implicated. The patient suffered no significant symptoms to the vaccine. When asked about if the medicine has an adverse effect on any aspect of the pregnancy, the reported stated it was unsure. The patient underwent lab tests and procedures which included covid-19 virus test: with result negative on 23Jan2021. The outcome of the event Miscarriage was recovered with sequel on 09Mar2021. This case was reported as serious with serious criteria- Other medically important condition by regulatory authority. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1422388 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Foreign  
Vaccinated:2021-03-06
Onset:2021-03-06
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Laboratory test, Macrocephaly, Maternal exposure during pregnancy, PTEN gene mutation, Stillbirth
SMQs:, Congenital, familial and genetic disorders (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? Yes
   Date died: 2021-06-12
   Days after onset: 97
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: biochemical tests; Result Unstructured Data: Test Result:PTEN Hamartoma tumor syndrome; Test Name: DNA tests; Result Unstructured Data: Test Result:PTEN Hamartoma tumor syndrome
CDC Split Type: ILPFIZER INC2021720556

Write-up: A genetic disease diagnosed by biochemical tests or DNA tests: PTEN Hamartoma tumor syndrome; Structural malformation: Macrocephaly; had a stillbirth on Saturday 12Jun2021, this is the 33rd week of pregnancy; a woman aged 35 had a stillbirth on Saturday 12Jun2021, this is the 33rd week of pregnancy; This is a spontaneous report from a contactable consumer (parent). This consumer reported information for both mother and fetus. This is a fetus report. A fetus patient mother (35-year-old) received bnt162b2 second single dose on 06Mar2021 (Batch/Lot number was not reported) for covid-19 immunisation at age of 35-year-old. The patient''s mother medical history and concomitant medications were not reported. The mother was vaccinated on 06Mar2021 with the second dose of the corona vaccine. She had a stillbirth on Saturday 12Jun2021, this was the 33rd week of pregnancy. A genetic disease diagnosed by biochemical tests or DNA tests: PTEN Hamartoma tumor syndrome and structural malformation was macrocephaly. It was not reported if an autopsy was performed. Information on the lot/batch number has been requested.; Sender''s Comments: Linked Report(s) : IL-PFIZER INC-2021720247 mother/fetus case; Reported Cause(s) of Death: a woman aged 35 had a stillbirth on Saturday 12Jun2021, this is the 33rd week of pregnancy; had a stillbirth on Saturday 12Jun2021, this is the 33rd week of pregnancy; A genetic disease diagnosed by biochemical tests or DNA tests: PTEN Hamartoma tumo


VAERS ID: 1098925 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Utah  
Vaccinated:2021-03-05
Onset:2021-03-07
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-03-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 RA / SYR

Administered by: School       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Haemorrhage in pregnancy, Ultrasound antenatal screen
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vitamin, Co-Q10 vitamin, and probiotics.
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: I just had an ultrasound on Tuesday March 9th.
CDC Split Type:

Write-up: I received the vaccination on Friday and on Sunday my bleeding increased. I already had some mild bleeding that had been constant since Feb 23rd or 24th. But I had an appointment on Feb 26th that confirmed I had a baby with a healthy heartbeat. I was also diagnosed with a very small uterine cyst. They told me the cause of the bleeding was pro ant implantation bleeding. I had light bleeding (bleeding just needing one or two pant liners each day) until Sunday the 7 when I saw an increase in bleeding. I called my doctor on Tuesday (I decided not to call Monday because I felt I would get the same answer I had already gotten, which was that everything was fine) and they had me come in die an urgent same day appointment. At that appointment I learned my baby did not have a heartbeat. The baby was measuring at just over 8 weeks. The due date given to me based on my last period was October 12th. So I was exactly 9 weeks when I went into the appointment Tuesday to find out the baby didn?t have a heartbeat. I officially miscarried the embryo and the placenta on Friday March 12th. This would have been my second baby. My first is a male and he is 18 months old. My first pregnancy didn?t have any complications. I do not have a history of miscarriage in my family, and this was the first one I have had. I did have to take 150mg of Clomid to get pregnant with this baby.


VAERS ID: 1170969 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-02-19
Onset:2021-03-07
   Days after vaccination:16
Submitted: 0000-00-00
Entered: 2021-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6200 / 2 LA / IM

Administered by: Military       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Exposure during pregnancy, Fatigue, Ultrasound scan
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: No
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data: Blood work, Ultrasound
CDC Split Type: vsafe

Write-up: I exp fatigue after Dose 2. I took a at home negative pregnancy test on 2/24 and I had positive test on 2/27. I miscarried on 3/7 which would have put me at 6 wks my estimated due date was the end of 10/2021.


VAERS ID: 1173008 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-02-28
Onset:2021-03-07
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ENG203 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Exposure during pregnancy, Ultrasound antenatal screen
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: No
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data: DNE, Blood work, 2 Ultrasounds
CDC Split Type: vsafe

Write-up: I had a miscarriage on 4/2 estimated and my estimated date of delivery 11/7/2021.


VAERS ID: 1311716 (history)  
Form: Version 2.0  
Age: 46.0  
Sex: Female  
Location: Illinois  
Vaccinated:2021-03-07
Onset:2021-03-07
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Fatigue, Full blood count, Gestational hypertension, Injection site pain, Injection site reaction, Platelet count decreased, Premature delivery, Subchorionic haematoma, Thrombocytopenia, Ultrasound foetal abnormal, Urticaria, Uterine hypertonus
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Haematopoietic thrombocytopenia (narrow), Haemorrhage terms (excl laboratory terms) (narrow), Systemic lupus erythematosus (broad), Extravasation events (injections, infusions and implants) (broad), Hypertension (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 4 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: heparin, norco, pyridoxine, aspirin
Current Illness: preterm contractions two weeks prior
Preexisting Conditions: paroxysmal atria tachycardia, sick sinus syndrome, lumbar spondylosis, arthritis, thrombophilia [compound heterozygote factor V leidein and prothrombin gene mutation], celiac disease
Allergies: adhesives, chlorhexidine, alcohol, pollen, procardia
Diagnostic Lab Data: CBC
CDC Split Type:

Write-up: Reported feeling fatigue and contractions early on after the second vaccine dose. Then the next day had pain and welts at heparin injection sites as well as increased contractions. Two days after vaccine went in for weekly fetal ultrasound and a large subamniotic hematoma [up to 7 cm in the greatest diameter] was found that was not present on ultrasound the week prior. There was mild thrombocytopenia on testing. Because of the hematoma providers did not want to continue anticoagulation. However due to an elevated risk of thrombosis due to a compound thrombophilia and pregnancy prolonged pregnancy without anticoagulation would also have a high risk for adverse outcomes. The decision was made for preterm delivery at 35 weeks. The postpartum course was complicated by postpartum hypertension. The newborn required an intensive care unit admission due to hypoxia within the first day of life and was found to have neonatal pneumonia.


VAERS ID: 1217133 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-25
Onset:2021-03-07
   Days after vaccination:41
Submitted: 0000-00-00
Entered: 2021-04-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 RA / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: ESPFIZER INC2021357991

Write-up: Missed abortion; This is a spontaneous report from a contactable other healthcare professional downloaded from the Regulatory Authority-WEB and received via Regulatory Authority ES-AEMPS-793140. A 30-year-old female patient received the second dose of BNT162B2 (COMIRANTY) (lot number/expiration date: not provided), via an unspecified route of administration, on 25Jan2021 as a single dose in the right arm for COVID-19 IMMUNIZATION. The patient previously patient received the first dose of BNT162B2 (COMIRANTY) (lot number/expiration date: not provided), via an unspecified route of administration, on 04Jan2021 as a single dose for COVID-19 IMMUNIZATION. Relevant medical history and concomitant medication were not provided. The patient (mother) was pregnant at the time of vaccination with date of last menstrual period (LMP) of 01Jan2021. Concomitant medication was not provided. On 07Mar2021, the patient experienced missed abortion. The clinical course is as follows: On 07Mar2021, the patient went to the emergency room for spotting less than a period. A deferred abortion was decided (uterine curettage). Treatment received for the event included uterine curettage. The outcome of the event missed abortion was recovering. No follow-up attempts possible. No further information expected. Lot/batch number was not provided and unable to obtain


VAERS ID: 1285077 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-04
Onset:2021-03-07
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-05-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EP2166 / 2 LA / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: THYREOIDINUM [THYROID]; FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Autoimmune thyroiditis; Pregnancy (induced delivery to term - live birth); Psoriatic arthritis (currently NOT active and not even symptomatic therapy)
Allergies:
Diagnostic Lab Data:
CDC Split Type: ITPFIZER INC2021342982

Write-up: miscarriage; This is a spontaneous report from a contactable physician downloaded from The regulatory authority number is IT-MINISAL02-704737. A 41-year-old female patient received the second dose of BNT162B2 (COMIRNATY, lot number: EP2166), via an unspecified route of administration, administered in the left arm (also reported as left shoulder), on 04Mar2021, as single dose, for COVID-19 immunisation. Medical history included autoimmune thyroiditis, psoriatic arthritis (currently not active and not even symptomatic therapy), got pregnant in 2019 (induced delivery to term-live birth, no previous miscarriages). Concomitant medications included thyroid (THYREOIDINUM) taken for autoimmune thyroiditis, and folic acid (FOLIC ACID), taken for an unspecified indication, both start and stop dates were not reported. The patient previously took apremilast (OTEZLA) for psoriatic arthritis; and estrogen-progestogen therapy many years ago. Historical vaccine included the first dose of BNT162B2 (COMIRNATY, lot number: EL0725), on 11Feb2021, for COVID-19 immunisation and experienced exposure during pregnancy. The patient''s last menstrual period was on 17Jan2021, gestation period was 7 weeks, due date was 24Oct2021. On 06Mar2021, symptoms (unspecified) started. On 07Mar2021, the patient experienced miscarriage. The patient recovered from the event on an unspecified date. Health Authority Comment: first dose 11Feb2021, second dose 04Mar2021, symptoms start on 06Mar2021, miscarriage on 07Mar2021. No follow-up attempts possible. No further information expected.


VAERS ID: 1573890 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Vermont  
Vaccinated:2021-01-11
Onset:2021-03-08
   Days after vaccination:56
Submitted: 0000-00-00
Entered: 2021-08-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 015M20A / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood prolactin normal, Blood thyroid stimulating hormone normal, Cardiolipin antibody negative, Exposure during pregnancy, Ultrasound antenatal screen abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: NKDA Hives to dogs when licked
Diagnostic Lab Data: Checked mother for anticardiolipin Abs, prolactin level, and TSH--all normal.
CDC Split Type:

Write-up: Pregnant at time of vaccination, confirmed by 8wk ultrasound with heartbeat on 1/29/21. Due date was . Missed miscarriage discovered at a routine ultrasound (nuchal translucency) at 13w2d on 3/8/21. Baby was a few days behind on measurements (so died within that week). No cause found but also no genetic testing done. No maternal illness or symptoms.


VAERS ID: 1582159 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Vermont  
Vaccinated:2021-02-11
Onset:2021-03-08
   Days after vaccination:25
Submitted: 0000-00-00
Entered: 2021-08-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 015M20A / 2 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed, Antinuclear antibody, Blood prolactin, Maternal exposure before pregnancy, Thyroid function test normal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamin
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: Tested prolactin, antiphospholipid Abs and TSH--all normal. Could not find cause for 13wk2d miscarriage.
CDC Split Type:

Write-up: Pregnant at time of vaccination, confirmed by 8wk ultrasound with heartbeat on 1/29/21. Due date was . Missed miscarriage discovered at a routine ultrasound (nuchal translucency) at 13w2d on 3/8/21. Baby was a few days behind on measurements (so died within that week). No cause found but also no genetic testing done. No maternal illness or symptoms. Also reported this for my 1st moderna vaccine


VAERS ID: 1854748 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-08
Onset:2021-03-08
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 013M20A / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Magnetic resonance imaging, Menstruation irregular, Ultrasound scan
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (broad)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: MRI, Ultrasound, order by Dr.
CDC Split Type:

Write-up: Has one son, eight. No previous miscarriages. 1 previous pregnancy (healthy). Suffered miscarriages at 8 weeks. No longer having regular periods.


VAERS ID: 1172172 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-01
Onset:2021-03-08
   Days after vaccination:35
Submitted: 0000-00-00
Entered: 2021-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Amenorrhoea, Ultrasound scan
SMQs:, Termination of pregnancy and risk of abortion (narrow), Fertility disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Hypothyroidism (substituted); Miscarriage
Allergies:
Diagnostic Lab Data: Test Date: 20210219; Test Name: Ultrasound; Result Unstructured Data: Test Result:good progress, fetal heart rate; Test Date: 20210308; Test Name: Ultrasound; Result Unstructured Data: Test Result:arrested pregnancy
CDC Split Type: FRPFIZER INC2021311649

Write-up: Early miscarriage; amenorrhea; This is a spontaneous report from a contactable physician downloaded from the regulatory authority number FR-AFSSAPS-TO20211552. A 41-year-old female patient received bnt162b2 (COMIRNATY), dose 2 intramuscular on 01Feb2021 (Batch/Lot number was not reported) as SINGLE DOSE (reported as 1 DF) for covid-19 immunisation. Medical history included hypothyroidism substituted, spontaneous miscarriage. The patient''s concomitant medications were not reported. The declaration is made by a doctor who is also the patient. The patient received D2 on February 1 (at 4 weeks gestation) and did not know she was pregnant. An ultrasound performed on 19Feb2021 confirmed good progress and a fetal heart rate. A new ultrasound performed on 08Mar2021 showed an arrested pregnancy at 8 weeks of amenorrhea and 4 days. Early miscarriage was reported. The patient was hospitalized and underwent general anesthesia for curettage on 10Mar2021. The mother reported she became pregnant while taking bnt162b2. The mother was due to deliver on 08Oct2021. Therapeutic measures were taken as a result of early miscarriage (abortion spontaneous). The events were assessed as serious (medically significant and hospitalization). The outcome of the events was recovered with sequel. No follow-up attempts possible. No further information expected. Batch/lot cannot be obtained.


VAERS ID: 1313359 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-13
Onset:2021-03-08
   Days after vaccination:23
Submitted: 0000-00-00
Entered: 2021-05-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: BEPFIZER INC2021484008

Write-up: Miscarriage, at 7 weeks and 2 days of pregnancy. Week before, still evolving pregnancy with a beating heart. Miscarriage on 08Mar2021.; This is a spontaneous report from a contactable physician downloaded from the Agency Regulatory Authority-WEB, regulatory authority number BE-FAMHP-DHH-N2021-83901. A 30-year-old female patient received BNT162B2 (COMIRNATY) on 13Feb2021 at single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient was pregnant at the time of vaccination: 1st trimester. The patient experienced miscarriage, at 7 weeks and 2 days of pregnancy. Week before, still evolving pregnancy with a beating heart. Miscarriage on 08Mar2021. It was reported that the vaccine may not be the cause. Patient was doing well. Baby died. The outcome of event was recovered on 08Mar2021. The event was reported as serious as medically significant. No follow-up attempts are possible, information on batch/lot number cannot be obtained.; Sender''s Comments: Event miscarriage represents an intercurrent medical condition and unrelated to BNT162B2 .


VAERS ID: 1362859 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2020-12-27
Onset:2021-03-08
   Days after vaccination:71
Submitted: 0000-00-00
Entered: 2021-06-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6796 / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed, Blood test, Maternal exposure during pregnancy, Ultrasound scan
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: Blood test; Result Unstructured Data: Test Result:Unknown results; Comments: No results available; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:Unknown results; Comments: No results available
CDC Split Type: DKPFIZER INC2021554013

Write-up: Maternal exposure during pregnancy; Missed abortion; This is a spontaneous report from a contactable physician downloaded from the RA-WEB DK-DKMA-WBS-0058177. Safety Report Unique Identifier DK-DKMA-ADR 24995005. A 36-year-old female patient received first dose of bnt162b2 (COMIRNATY, Lot number: EJ6796, Expiration Date: 30Apr2021) intramuscular on 27Dec2020 at single dose for COVID-19 immunisation. Medical history and concomitant medication were not provided. Patient experienced missed abortion and maternal exposure during pregnancy. On 08Mar2021, the patient was diagnosed with missed abortion. The patient was not recognized pregnant at the time of vaccination. The ADRs (adverse drug reactions) were by the reporter reported as resulting in hospitalisation. The patient underwent lab tests and procedures, which included blood test: No results available; ultrasound scan: No results available. Treatment or medical procedure due to the events were not reported. Outcome of the event missed abortion was not recovered, outcome of the event maternal exposure during pregnancy was recovered. No follow-up attempts possible. No further information expected.


VAERS ID: 1104712 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-03-06
Onset:2021-03-09
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-03-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 014M20A / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage after vaccine. I was 11 weeks pregnant. Estimated date of delivery is 9/20/21.


VAERS ID: 1117511 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-02-12
Onset:2021-03-09
   Days after vaccination:25
Submitted: 0000-00-00
Entered: 2021-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / -

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Human chorionic gonadotropin
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: HCG labs: 3/10 and 3/16
CDC Split Type:

Write-up: Adverse event: miscarriage Estimated date of delivery: October 2021 Pregnancy history: two previous pregnancies, carried full term, vaginal deliveries, healthy


VAERS ID: 1130798 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Mississippi  
Vaccinated:2021-02-02
Onset:2021-03-09
   Days after vaccination:35
Submitted: 0000-00-00
Entered: 2021-03-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 030L20A / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, First trimester pregnancy, Laboratory test, Ultrasound Doppler
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: OTC - Iron, Prenatal Vitamin, Vitamin C
Current Illness: None
Preexisting Conditions: None
Allergies: NA
Diagnostic Lab Data: I had an ultrasound & labs done on 3/12 at Hospital. Repeat labs done on 3/15 at Hospital. Repeat ultrasound done on 3/16 at Physician''s & Surgeon''s Clinic.
CDC Split Type:

Write-up: I did not know at the time of the 2nd shot, but I was pregnant. I miscarried on 3/12. I was approximately 11 weeks pregnant.


VAERS ID: 1407174 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Maine  
Vaccinated:2021-01-26
Onset:2021-03-09
   Days after vaccination:42
Submitted: 0000-00-00
Entered: 2021-06-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 013L20A / 2 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Haemorrhage, Laboratory test, Ultrasound scan, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamin and vitamin c
Current Illness: none
Preexisting Conditions: exercise induced asthma
Allergies: none
Diagnostic Lab Data: ER visit, Lab work, and ultrasounds.
CDC Split Type:

Write-up: The morning before my second Moderna vaccine I took a pregnancy test and it was inconclusive so I figured I wasn''t pregnant and got my second vaccine (1/26/21). I missed my period and took another pregnancy test on 1/30/21 and it was positive. I went to my first ultrasound on 3/2/21 when I should have been around 8 or 9 weeks and the baby was measuring small but it had a heart beat that was in a normal range. A week later on 3/9/21 I started spotting and I called my doctor and they told me to let them know if it got worse. I went to work but by the end of my shift the bleeding had got worse and my doctor made me go to the ER so I could have another ultrasound. The ultra sound showed the baby still had a heart rate but it was low. I stayed home from work the next day to take it easy and I ended up having a miscarrage that night 3/10/21. I had a follow up ultrasound on 3/11/21 that proved it. I wasn''t planning on reporting this because really anything could have caused it but I signed up for the vaccine app when I got my vaccines and answered the follow up questions. Someone called me because of how I answered my question and she recommended that I report it.


VAERS ID: 1165551 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Foreign  
Vaccinated:2021-01-29
Onset:2021-03-09
   Days after vaccination:39
Submitted: 0000-00-00
Entered: 2021-04-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6795 / 2 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Anembryonic gestation, Maternal exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: PARACETAMOL; TEMAZEPAM; IBUPROFEN
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLPFIZER INC2021352904

Write-up: Maternal exposure during pregnancy; Blighted ovum; Miscarriage; This is a spontaneous report from a contactable consumer downloaded from the regulatory authority NL-LRB-00472449. This consumer reported information for both mother and fetus. This is the fetus report. This serious spontaneous report from a contactable consumer (patient mother). A fetus patient of unspecified gender received bnt162b2 (COMIRNATY) via transplacental route, when the patient''s mother received the 2nd dose of BNT162B2 (COMIRNATY, lot number: EJ6795) vaccine via an unspecified route of administration on 29Jan2021 at single dose for covid-19 immunisation. Medical history was unknown. Concomitant medications included paracetamol, temazepam and ibuprofen. Shortly after the 2nd vaccination the patient''s mother turned out to be pregnant, conception date was 28Jan2021. So 1 day before the 2nd vaccine. On 09Mar2021, the patient''s mother was found out at 8 weeks of pregnancy that the fetus probably stopped growing at a very early stage, a so-called blighted ovum. It was not known exactly when. Blighted ovum was treated with Induce miscarriage tomorrow with misoprostol and miscarriage was treated with induce miscarriage tomorrow with misoprostol. Gynecologist thought in the first week. The patient''s mother personally think that the miscarriage was not the result of the vaccination, but patient''s mother cannot rule it out. Outcome of the events was unknown. This report was reported as serious. No follow-up attempts are needed. No further information is expected.; Sender''s Comments: Linked Report(s) : NL-PFIZER INC-2021297561 maternal/fetus case


VAERS ID: 1183813 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-13
Onset:2021-03-09
   Days after vaccination:55
Submitted: 0000-00-00
Entered: 2021-04-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK1868 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure during breast feeding, SARS-CoV-2 test
SMQs:, Neonatal exposures via breast milk (narrow), Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: SERETIDE
Current Illness: Breast feeding
Preexisting Conditions: Medical History/Concurrent Conditions: Asthma
Allergies:
Diagnostic Lab Data: Test Date: 20200728; Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021357843

Write-up: Maternal exposure during breast feeding; Early miscarriage; This is a spontaneous from a contactable consumer downloaded from the Medicines Agency (MA) WEB GB-MHRA-WEBCOVID-202103261729284690. A 40-Year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EK1868) via an unspecified route of administration on 13Jan2021 at a single dose and second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EM4965) via an unspecified route of administration on 24Mar2021 at a single dose for COVID-19 immunization. Patient''s medical history included breast feeding ongoing and asthma. Concomitant medication included fluticasone propionate, salmeterol xinafoate (SERETIDE) for asthma. On 09Mar2021the patient experienced early miscarriage and on an unspecified date maternal exposure during breast feeding. The Patient has not had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. The patient underwent lab test and procedure which included COVID-19 virus test: negative on 28Jul2020. The outcome of early miscarriage was recovered on 14Mar2021 and for other event was unknown. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1089690 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2021-03-01
Onset:2021-03-10
   Days after vaccination:9
Submitted: 0000-00-00
Entered: 2021-03-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: Seafood
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage


VAERS ID: 1110463 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-02-18
Onset:2021-03-10
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-03-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 038K20A / 2 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage determined at 19 weeks gestation on 3/10/2021.


VAERS ID: 1234210 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Indiana  
Vaccinated:2021-03-03
Onset:2021-03-10
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-04-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011J20A / 1 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Intermenstrual bleeding
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: N/A
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: The patient received the first vaccine on 03MAR21 and began spotting on 10MAR21. A miscarriage was confirmed on 19MAR21. At the time of the first vaccine (03MAR21) the patient was unaware that she was pregnant as she had a negative home pregnancy test on 02MAR21. She was told by her OB/GYN to inform us of her miscarriage.


VAERS ID: 1257703 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-02-18
Onset:2021-03-10
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-04-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6200 / 1 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Complication of pregnancy, Exposure during pregnancy, Gestational hypertension, Premature delivery
SMQs:, Hypertension (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient had elevated blood pressure affecting pregnancy. Her cesarean section due date was moved up from 3/22 to 3/10. Per notes from Doctor on 3/10/21: Estimated Date of Delivery: 3/28/21 who presented for repeat C/S at 37 wks due to GHTN. Her BP''s did normalize following delivery and she did not require antihypertensive medications. Procedure was uncomplicated as was her postoperative stay. Baby did get admitted to NICU and is doing well.


VAERS ID: 1333297 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Connecticut  
Vaccinated:2021-01-28
Onset:2021-03-10
   Days after vaccination:41
Submitted: 0000-00-00
Entered: 2021-05-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 028L20A / 2 LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound scan
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal
Current Illness: none
Preexisting Conditions: none
Allergies: Avelox- hives
Diagnostic Lab Data: 3/8/21: transvaginal ultrasound which confirmed pregnancy 3/8/21: HCG 1956, progesterone 3.47 3/10/21: HCG 1467, progesterone 1.88 3/16/21: transvaginal ultrasound which showed complete spontaneous miscarriage
CDC Split Type:

Write-up: Rec''d 2nd COVID vaccine on 01/28/21. Positive pregnancy test on 2/14/21 with estimated due date 10/26/21. On 3/5/21 scant spotting noted. Contacted OBGYN on 3/8/21, seen in the office. Ultrasound confirmed intrauterine pregnancy with gestation sac, yolk sac and possible fetal pole although measuring smaller than estimated due date. HCG/Progesterone levels drawn. Repeat HCG/progesterone levels drawn on 3/10/21 showed decline. Started miscarrying 3/10/21 morning following blood work. Seen again in OBGYN office 3/16/21 which confirmed complete spontaneous miscarriage.


VAERS ID: 1808129 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Kentucky  
Vaccinated:2021-03-05
Onset:2021-03-10
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 003A21A / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure before pregnancy, Menstruation irregular, Pregnancy test positive, SARS-CoV-2 test positive, Ultrasound scan
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Fertility disorders (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: July 9th Covid 19 -Positive Pregnancy Test- Positive July 13th -Ultrasound- heartbeat Aug 10th -Ultrasound- no heartbeat Oct 1st -D and C
CDC Split Type:

Write-up: My menstruation was not regular. I have always had a very regular menstrual cycle. My menstruation has always been between 26-28 days. After the Moderna vaccine, the first month was 34 days and the second month was 36 days and third month was 21 days cycle. The fourth month after receiving my first vaccine was normal 28 days. This period started May 31st. In June, I became pregnant. I did not know I was pregnant until the beginning of July. My husband tested positive for Covid on June 26th. Towards the end of our quarantining, I tested positive for Covid-19 on July 9th. I started bleeding this same day. I went to the doctor on July 13th after my quarantine was over. They confirmed the pregnancy and ultrasound detected a heartbeat. A month later I went back to the doctor, and they informed me that I had miscarried that baby less than a week after I went to the doctor in July.


VAERS ID: 1311643 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-19
Onset:2021-03-10
   Days after vaccination:19
Submitted: 0000-00-00
Entered: 2021-05-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER0641 / 2 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Fibrin D dimer, Human chorionic gonadotropin
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Polycystic ovaries
Allergies:
Diagnostic Lab Data: Test Date: 20201212; Test Name: DDR; Result Unstructured Data: Test Result:unknown results; Test Date: 20210130; Test Name: BETA HCG; Result Unstructured Data: Test Result:39349.7 IU/l; Comments: 7 weeks; Test Date: 20210217; Test Name: BETA HCG; Result Unstructured Data: Test Result:73551.8 IU/l; Comments: (9 weeks + 4days); Test Date: 20210219; Test Name: BETA HCG; Result Unstructured Data: Test Result:66713.8 IU/l
CDC Split Type: FRPFIZER INC2021478330

Write-up: Miscarriage; This is a spontaneous report from a contactable physician downloaded from an Agency- WEB FR-AFSSAPS-TO20212702, Safety Report Unique Identifier FR-AFSSAPS-2021040220 received via regulatory authority. A 25-year-old female patient received bnt162b2 (COMIRNATY), dose 1 via an unspecified route of administration on 25Jan2021 (Batch/Lot number was not reported) as single dose, dose 2 intramuscular on 19Feb2021 (Batch/Lot Number: ER0641) as single dose for covid-19 immunisation. Medical history included polycystic ovaries. The patient''s concomitant medications were not reported. Long-term treatment: None. The patient experienced miscarriage on 10Mar2021 with outcome of recovered with sequelae on 10Mar2021. Clinical signs: As part of the COVID-19 vaccination, the patient received a first injection on 25Jan2021 while she was 6 weeks + 2 days pregnant, and the second injection on 19Feb2021 at 9 weeks + 6J. It was a twin pregnancy, complicated by the loss of a first embryo at the start of pregnancy (exact date not known). Biology: 30Jan2021 (7 weeks): Serum BETA HCG dosage = 39,349.7 IU / L, 17Feb2021 (9 weeks + 4days): Serum BETA HCG dosage = 73,551.8 IU / L, 19Feb2021 (9 weeks + 4days) (as reported): Serum BETA HCG dosage = 66,713.8 IU/L. Evolution: The patient had a miscarriage on 10Mar2021 at 12 Weeks + 4Days. Comments: DDR (D-dimer during pregnancy): 12Dec2020, DDG (Gestational diabetes): 26Dec2020. Expected end date: 26Sep2021. No follow-up attempts possible. No further information expected.; Sender''s Comments: Linked Report(s) : FR-AFSSAPS-TO20212702 AFSSAPS;FR-AFSSAPS-2021040220 AFSSAPS


VAERS ID: 1418860 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-03-10
Submitted: 0000-00-00
Entered: 2021-06-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH NOT KNOWN / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, SARS-CoV-2 test
SMQs:, Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: Patient has not had symptoms associated with COVID-19 Patient is not enrolled in clinical trial
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021663990

Write-up: Pregnancy loss; This is a spontaneous report from a contactable consumer or other non hcp received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202106061817115130-O3CQH. Sender''s (Case) Safety Report Unique Identifier: GB-MHRA-ADR 25427601. A female patient of an unspecified age received bnt162b2 (COVID-19 MRNA VACCINE BIONTECH; Batch/lot number: Not known), via an unspecified route of administration on an unspecified date as DOSE 1, SINGLE for covid-19 immunisation. Patient''s medical history and concomitant medications were not reported. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. The patient experienced pregnancy loss on 10Mar2021. The event was assessed as serious (medically significant and disability). Patient has not tested positive for COVID-19 since having the vaccine. The patient underwent lab tests and procedures which included COVID-19 virus test with result of ''no - negative covid-19 test'' on an unspecified date. Outcome of the event was recovered/resolved with sequel. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1706189 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-10
Onset:2021-03-10
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-09-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ET9096 / 1 LA / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed, Human chorionic gonadotropin, Intermenstrual bleeding, Pregnancy on oral contraceptive
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: MARVELON 28
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 202108; Test Name: Blood human chorionic gonadotropin; Result Unstructured Data: Test Result:Low/reduced
CDC Split Type: NOPFIZER INC202101143070

Write-up: She is not sure when she had her last menstruation. She had a small bleeding (2-3 days) two weeks after her first dose of Comirnaty.; Missed Abortion; PREGNANCY ON ORAL CONTRACEPTIVE; This is a spontaneous report from a contactable other hcp downloaded from the Regulatory Authority-WEB, regulatory authority number NO-NOMAADVRE-FHI-2021-Un32yz. A 39-years-old female patient received bnt162b2 (COMIRNATY), intramuscular, administered in Arm Left on 10Mar2021 at 39-years-old (Batch/Lot Number: ET9096) as dose 1, single for covid-19 immunisation. The patient medical history irregular menstruation cycle. Concomitant medications included desogestrel, ethinylestradiol (MARVELON 28) taken for contraception, start and stop date were not reported. Marvelon used for 15-20 years with good effect/no problems. Compliant and no missed tablets of Marvelon. On 10Mar2021, the patient developed pregnancy on oral contraceptive, missed abortion. Got pregnant on oral contraceptive pills. The reporter is convinced that it is the vaccine that is the reason / to blame for the contraception not working as it should when she became pregnant, ended with aborted pregnancy. Relevant laboratory findings and investigations included in the report (blood human chorionic gonadotropin, aug2021, low/reduced). She is not sure when she had her last menstruation. She had a small bleeding (2-3 days) two weeks after her first dose of Comirnaty. The last two years her menstruation cycle has been a little irregular, so she was starting to suspect she was approaching menopause. At first she didn''t react when she missed her menstruation, since she used Marvelon and had irregular menstruation the last two year''s. Therefore, it took a long time before she realized she was pregnant. However, she got pregnant despite compliant use of Marvelon. She was followed up by a midwife during pregnancy. At consultation with her midwife in August her blood hormone level was low, a bad sign according to the midwife, and she was referred to hospital. On 16Aug2021, Missed abortion was detected at the hospital, probably in pregnancy week 12-15. No other known reasons for lack of effect of Marvelon. She has had good effect of Marvelon for 15-20 years. The outcome of the events was unknown. The patient took dose 2 of Comirnaty on 31Mar2021, Intramuscular, Batch/lot number: ET9096. The case was considered to be Serious. Relatedness of drug to reactions/events Comirnaty/ all events/ Regional Pharmacovigilance Center/ Possible. Reporter''s comments: Health worker No follow-up attempts are needed. No further information is expected.; Reporter''s Comments: Health worker


VAERS ID: 1099240 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: New York  
Vaccinated:2020-12-30
Onset:2021-03-11
   Days after vaccination:71
Submitted: 0000-00-00
Entered: 2021-03-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Human chorionic gonadotropin
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal
Current Illness: None
Preexisting Conditions: Mild intermittent asthma, season and environmental allergies
Allergies: Aspirin, nsaids, sulfa
Diagnostic Lab Data: Serial hcg on 3/4/2020 and 3/11/2020
CDC Split Type:

Write-up: Complete spontaneous Miscarriage at 6 weeks and 5 days


VAERS ID: 1108805 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-03-03
Onset:2021-03-11
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-03-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Exposure during pregnancy, Premature delivery, Premature rupture of membranes
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 6 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Sertraline 100 mg, vitamin D 5000 IU, omeprazole, bonjesta, prenatal vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: 28 weeks 6 days pregnant, Preterm rupture of the membrane. Admitted to the hospital at 29 weeks. Delivered at 29 weeks 4 days. Pregnancy was an IVF pregnancy with no other complications. Baby delivered on 3/16 and weighed 3 pounds 7 ounces.


VAERS ID: 1118882 (history)  
Form: Version 2.0  
Age: 50.0  
Sex: Female  
Location: Louisiana  
Vaccinated:2021-02-25
Onset:2021-03-11
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-03-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6203 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6208 / 2 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound abdomen abnormal
SMQs:, Retroperitoneal fibrosis (broad), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: l-thyroxine 100 mcg, prenatal vitamin, estrogen (6 mg/day) & progesterone in oil (1 ml IM per day), as per reproductive endocrinologist prescribed protocol
Current Illness: N/A
Preexisting Conditions: hypothyroidism
Allergies: N/A
Diagnostic Lab Data: Ultrasounds showed no fetal activity at 7 weeks gestation (transferring 5-day blastocyst = 2 weeks gestation at time of transfer)
CDC Split Type:

Write-up: I had a double frozen embryo transfer on February 5th and a positive pregnancy test on February 15th. On March 4th I had my 6-week ultrasound and one embryo had implanted but did not survive and the 2nd was clearly not strong, smaller than it should have been with a fetal heartbeat only visible, not audible yet. A week later, on March 11th, the ultrasound showed only empty gestational sacs and I had miscarried both.


VAERS ID: 1177795 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Tennessee  
Vaccinated:2021-03-08
Onset:2021-03-11
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-04-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound scan, Uterine dilation and curettage
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Labeltol, previcid, prenatal vitamins, unisom
Current Illness:
Preexisting Conditions: Lupus
Allergies: None
Diagnostic Lab Data: Ultrasound 3/11 Ultrasound 3/16 D&C 3/19
CDC Split Type:

Write-up: Miscarried found no fetal heartbeat at 3/11 ultrasound. D&C completed 3/19


VAERS ID: 1347913 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-02-13
Onset:2021-03-11
   Days after vaccination:26
Submitted: 0000-00-00
Entered: 2021-05-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Ovulation disorder, Pregnancy, Uterine spasm
SMQs:, Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: The first Moderna shot caused me to miss my next menstrual cycle, which had never happened to me prior to receiving the shot. In the week I received the 2nd shot on 3/13/21, I had uterine cramping that same day within a few hours of getting the shot. I also noticed a change to my cervical mucus during my ovulation cycle 2 weeks later. I then became pregnant the following month and was found to have a missed miscarriage at 6 weeks 1 day. It seems like their is a strong correlation between the side effects from the Moderna shot and the miscarriage.


VAERS ID: 1425776 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-02-13
Onset:2021-03-11
   Days after vaccination:26
Submitted: 0000-00-00
Entered: 2021-06-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Amenorrhoea, Ovulation disorder, Pregnancy, Uterine spasm
SMQs:, Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: No adverse event (Medical history not reported)
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20212

Write-up: Amenorrhoea; Abortion spontaneous; Ovulation disorder; Pregnancy; Uterine spasm; This case was received via VAERS on 15-Jun-2021 and was forwarded to Moderna on 15-Jun-2021. This regulatory authority pregnancy case was reported by an other health care professional and describes the occurrence of ABORTION SPONTANEOUS (Abortion spontaneous) in a 29-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 13-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On 11-Mar-2021, the patient experienced ABORTION SPONTANEOUS (Abortion spontaneous) (seriousness criterion medically significant), OVULATION DISORDER (Ovulation disorder), PREGNANCY (Pregnancy) and UTERINE SPASM (Uterine spasm). On an unknown date, the patient experienced AMENORRHOEA (Amenorrhoea). At the time of the report, ABORTION SPONTANEOUS (Abortion spontaneous), OVULATION DISORDER (Ovulation disorder), PREGNANCY (Pregnancy), UTERINE SPASM (Uterine spasm) and AMENORRHOEA (Amenorrhoea) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided by the provided. No treatment information was provided. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) was not applicable.; Sender''s Comments: This is a case of product exposure during pregnancy which resulted in Abortion spontaneous, for this 29 years old female. Very limited information has been provided at this time.


VAERS ID: 1275599 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-23
Onset:2021-03-11
   Days after vaccination:47
Submitted: 0000-00-00
Entered: 2021-04-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0739 / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Folic acid deficiency
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021424805

Write-up: Maternal exposure during pregnancy; Miscarriage; This is a non-interventional study report from a contactable pharmacist and a contactable consumer. This is a report received from the Regulatory Authority, report number is GB-MHRA-YCVM-202104162110581930 with the Safety Report Unique Identifier of GB-MHRA-ADR 25154208. A 32-year-old pregnant female patient received BNT162b2 (COVID-19 MRNA VACCINE BIONTECH, Lot Number: EL0739), via an unspecified route of administration on 23Jan2021 at single dose for COVID-19 immunization. The patient is not currently breastfeeding. Medical history included folate deficiency. Concomitant medication included folic acid (manufacturer unknown) taken for vitamin supplementation. Since the vaccination, the patient had not been tested for COVID-19. The patient had not had symptoms associated with COVID-19 and was not enrolled in the clinical trial. On an unspecified date, the patient reported that she became pregnant while taking BNT162B2 (maternal exposure during pregnancy). Patient''s last menstrual period date was on 21Jan2021 and she was due to deliver on 28Oct2021 (the estimated due date). On 11Mar2021, the patient had a miscarriage and she was 7 weeks pregnant. On 14Apr2021, the patient''s scan showed empty womb after miscarriage. The clinical outcome of the maternal exposure during pregnancy resolved on 11Mar2021. The patient had recovered from the miscarriage on 14Apr2021. The reporter''s assessment of the causal relationship of the events with suspect product, BNT162b2 was not provided at the time of this report. Since no determination has been received, the case is managed based on the company causality assessment. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: The Company cannot completely exclude the possible causality between the reported miscarriage, exposure during pregnancy and the administration of the COVID 19 vaccine, BNT162B2, based on the known safety profile and reasonable temporal association. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1458165 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-26
Onset:2021-03-11
   Days after vaccination:13
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER1741 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure during pregnancy, SARS-CoV-2 test
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Folic acid supplementation; Lactation decreased; Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021776395

Write-up: Maternal exposure during pregnancy/ Patient was exposed to the medicine first-trimester (1-12 weeks).; Miscarriage; This is a spontaneous report from a contactable consumer. This is a report received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-WEBCOVID-202106231043155490-YC1NB, Safety Report Unique Identifier GB-MHRA-ADR 25524457. A 32-years-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number ER1741), via an unspecified route of administration on 26Feb2021 at single dose for COVID-19 immunization. Medical history included lactation decreased, pregnancy not ongoing, patient no longer pregnant at the time of reporting, folic acid supplementation. Patient had not had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. Patient was not currently breastfeeding. Concomitant medication included folic acid taken for folic acid supplementation. The patient experienced maternal exposure during pregnancy on an unspecified date, miscarriage on 11Mar2021. Patient was exposed to the medicine first-trimester (1-12 weeks). Case was reported as serious, medically significant. The patient underwent lab tests and procedures which included sars-cov-2 test: negative, No - Negative COVID-19 test. Outcome of miscarriage was recovered on 15Mar2021 and the other event was unknown. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1490182 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-07
Onset:2021-03-11
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-07-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EP2163 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion induced, Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Basedow''s disease; Thyroidectomy
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEPFIZER INC2021843191

Write-up: Miscarriage/missed abortion in the 10th week of pregnancy; biochemical termination of pregnancy in the 5th week of pregnancy; This is a spontaneous report from a non-contactable physician downloaded from the WEB, regulatory authority number DE-PEI-202100118676. A pregnant female patient of an unspecified age received bnt162b2 (COMIRNATY, Lot Number: EP2163), via an unspecified route of administration on 07Mar2021 as dose 2, 0.3 mL single for COVID-19 immunization. Medical history included Basedow''s disease and thyroidectomy both from an unknown date. The patient''s concomitant medications were not reported. The patient previously received the first dose of bnt162b2 (COMIRNATY, Lot Number: EL5723) on 14Feb2021 for COVID-19 immunization. On 11Mar2021, it was reported that the patient experienced biochemical termination of pregnancy in the 5th week of pregnancy and on 21May2021 had miscarriage/missed abortion in the 10th week of pregnancy. The mother was 5 weeks pregnant at the onset of the event. The pregnancy resulted in spontaneous abortion. The fetal outcome is intrauterine death. The reporter assessed the events as serious. The outcome of the events was unknown. Sender''s comments: Abrasion in missed abortion state after thyroidectomy. No follow-up attempts possible. No further information expected.


VAERS ID: 1853040 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-08
Onset:2021-03-11
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW9127 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Haemorrhage, Maternal exposure during pregnancy
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: SEPFIZER INC202101438128

Write-up: Miscarriage; miscarriage with a heavy bleeding; Maternal exposure during pregnancy, first trimester; This is a spontaneous report from a contactable nurse downloaded from the Regulatory Authority, regulatory authority number SE-MPA-2021-089646, with Safety Report Unique Identifier SE-VISMA-1634097504626. This is a mother report. A 43-year-old female patient received bnt162b2, dose 2 via an unspecified route of administration on 08Apr2021 (Lot Number: EW9127) as DOSE 2, SINGLE; dose 1 via an unspecified route of administration on 11Mar2021 (Lot Number: EP2166) as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history was not reported. The patient''s concomitant medications were not reported. A woman with three children and no history of prior miscarriages, who received her first dose of vaccination in close connection to conception, about pregnancy week one. The second dose was administered around pregnancy week five, whereafter the woman became aware of the pregnancy the following week. Around pregnancy week 12 the woman suffered from a miscarriage with a heavy bleeding, therefore she was hospitalised. Events were reported as serious with medically significant and hospitalization. The outcome of the events was unknown.; Sender''s Comments: Linked Report(s) : SE-PFIZER INC-202101447656 same patient, different dose and event


VAERS ID: 1097975 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-03-11
Onset:2021-03-12
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-03-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Haemorrhage, Ultrasound antenatal screen abnormal
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamin
Current Illness: none
Preexisting Conditions: fibroid
Allergies: gluten intolerant, no known medication allergies
Diagnostic Lab Data: blood draws and ultrasounds to assess and confirm the diagnosis
CDC Split Type:

Write-up: Patient started having pain prior to her injection on 3/11/21. On 3/12/21, she started bleeding, and on 3/14/21 she miscarried at 13 weeks.


VAERS ID: 1117428 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Indiana  
Vaccinated:2021-01-30
Onset:2021-03-12
   Days after vaccination:41
Submitted: 0000-00-00
Entered: 2021-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 030L20A / 1 LA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Anembryonic gestation, Exposure during pregnancy, Human chorionic gonadotropin decreased, Multigravida, Ultrasound antenatal screen abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: Amoxicillin
Diagnostic Lab Data: Ultrasound on 3-12-21 with empty gestational sac Blood tests performed with dropping hcg levels on 3-12-21 and 48hrs later on 3-14-21
CDC Split Type:

Write-up: I miscarried with a blighted ovum. Pregnancy history. I have no medical conditions and have had 2 healthy pregnancies prior. I had the first vaccine the week I ovulated and then found out I was pregnant the following month. Jan 19th was the date of my last menstrual cycle Est il mated date of delivery: oct 26, 2021


VAERS ID: 1184480 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Michigan  
Vaccinated:2020-12-29
Onset:2021-03-12
   Days after vaccination:73
Submitted: 0000-00-00
Entered: 2021-04-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / SC

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: Sunflower oil, skin allergy only
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage


VAERS ID: 1235494 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Wisconsin  
Vaccinated:2021-02-12
Onset:2021-03-12
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-04-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Fatigue, Feeling abnormal, Foetal heart rate abnormal, Headache, Malaise, Pain in extremity, Ultrasound foetal abnormal, Ultrasound scan, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Dementia (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FLUOXETINE; PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS ; CYTOTEC
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Anxiety
Allergies:
Diagnostic Lab Data: Test Date: 20210325; Test Name: Ultrasound; Result Unstructured Data: Had some bleeding and found out it was subchorionic hemorrhage. Bleeding is in another part of the uterus where is baby is not; Test Date: 20210401; Test Name: Ultrasound; Result Unstructured Data: Saw baby heartbeat but was informed baby had not grown
CDC Split Type: USMODERNATX, INC.MOD20210

Write-up: pain in arm; Miscarried; No fetal heartbeat.; Menstrual bleeding; Pregnant; General sick and tired feeling; Did not want to get out of bed; Pretty tired; Headache; This spontaneous prospective pregnancy case was reported by a consumer and describes the occurrence of ABORTION SPONTANEOUS (Miscarried) in a 25-year-old female patient (gravida 1, para 1) who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included Anxiety on 01-Jan-2010. Concomitant products included FLUOXETINE for Anxiety, PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS FUMARATE;FOLIC ACID;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RETINOL ACETATE;RIBOFLAVIN;THIAMINE MONONITRATE;TOCOPHERYL ACETATE;ZINC OXIDE] for Pregnancy, MISOPROSTOL (CYTOTEC) for an unknown indication. On 12-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. The patient''s last menstrual period was on an unknown date and the estimated date of delivery was 15-Nov-2021. On 12-Mar-2021, the patient experienced EXPOSURE DURING PREGNANCY (Pregnant). 12-Mar-2021, the patient experienced MALAISE (General sick and tired feeling), FEELING ABNORMAL (Did not want to get out of bed), FATIGUE (Pretty tired) and HEADACHE (Headache). On 22-Mar-2021, the patient experienced VAGINAL HAEMORRHAGE (Menstrual bleeding). On 01-Apr-2021, the patient experienced FOETAL GROWTH ABNORMALITY (Baby had not grown). On 09-Apr-2021, the patient experienced ABORTION SPONTANEOUS (Miscarried) (seriousness criterion medically significant), FOETAL HEART RATE ABNORMAL (No fetal heartbeat.) and HEREDITARY DISORDER (Genetic issue). On 12-Mar-2021, EXPOSURE DURING PREGNANCY (Pregnant) had resolved. On 09-Apr-2021, ABORTION SPONTANEOUS (Miscarried), FOETAL GROWTH ABNORMALITY (Baby had not grown) and FOETAL HEART RATE ABNORMAL (No fetal heartbeat.) had resolved. At the time of the report, VAGINAL HAEMORRHAGE (Menstrual bleeding), MALAISE (General sick and tired feeling), FEELING ABNORMAL (Did not want to get out of bed), HEREDITARY DISORDER (Genetic issue), FATIGUE (Pretty tired) and HEADACHE (Headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 25-Mar-2021, Ultrasound foetal abnormal: abnormal (abnormal) Had some bleeding and found out it was subchorionic hemorrhage. Bleeding is in another part of the uterus where is baby is not. On 01-Apr-2021, Ultrasound scan: abnormal (abnormal) Saw baby heartbeat but was informed baby had not grown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment information provided mentioned ultrasound and cytotec. Action taken with mRNA-1273 in response to the event was not applicable as patient took both doses of the vaccine. Patient reported that she does not blame Moderna, as her OB feels the miscarriage was related to a "genetic issue. This case was linked to MOD-2021-060699 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 13-Apr-2021: Patient updated AE and mentions fetal complications resulting in miscarriage. Events and outcome of case thus updated with new information.; Sender''s Comments: Based on the current available information and the temporal association between the product use and the start date of the events a causal relationship cannot be excluded.


VAERS ID: 1186005 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-03-09
Onset:2021-03-13
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-04-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6199 / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Haemorrhage, Human chorionic gonadotropin decreased, Pregnancy test positive
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins Thorne and supplements for Calcium Magnesium, Iron, Fish Oil, Vitamin C, Zinc,
Current Illness: n/a
Preexisting Conditions: n/a
Allergies: None known
Diagnostic Lab Data: Pregnancy Test 3/16 positive Hcg blood level tests 3/17, 3/24, 3/31, 4/9 show decreasing levels of hcg
CDC Split Type:

Write-up: I experienced a miscarriage that started with bleeding on 3/13 and was confirmed by ongoing hcg level tests starting on 3/17. I passed a lot of blood and blood tissue in an intense event on 3/16. I did not know I was pregnant at the time and was estimated to be around 9-10 weeks (due date around October 2021) based on hcg levels. I was also breastfeeding at the time of my vaccine. I was advised to go to the emergency room if certain conditions occurred including extreme pain -- I opted to go to Urgent Care that evening to get checked out and to get a blood hcg test. Urgent care was unable to do the blood test and they recommended I call my provider the next day or go to the Emergency Department if certain symptoms occurred.


VAERS ID: 1225179 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-01-11
Onset:2021-03-13
   Days after vaccination:61
Submitted: 0000-00-00
Entered: 2021-04-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 AR / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure before pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin, Zyrtec
Current Illness:
Preexisting Conditions:
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage 2 months after vaccine


VAERS ID: 1759642 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Ohio  
Vaccinated:2020-12-26
Onset:2021-03-13
   Days after vaccination:77
Submitted: 0000-00-00
Entered: 2021-10-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK5730 / 1 RA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK9231 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure before pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: pre natal vitamin
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Spontaneous misscarriage


VAERS ID: 1473427 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-03-13
Submitted: 0000-00-00
Entered: 2021-07-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure during pregnancy, Ultrasound scan
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Folic acid supplementation; Miscarriage; Pregnancy (Patient no longer pregnant at the time of reporting.); Pregnancy (Details of previous pregnancies: 2017 Live male); Pregnancy (Details of previous pregnancies: 2014 Live Female)
Allergies:
Diagnostic Lab Data: Test Name: Ultrasound; Result Unstructured Data: Test Result:MISSED MISCARRIAGE; Comments: Missed miscarriage at 11weeks (7week size on USS)
CDC Split Type: GBPFIZER INC2021829640

Write-up: Maternal exposure during pregnancy; Miscarriage; This is a spontaneous report from a contactable consumer or other non hcp received from the Regulatory Authority. The regulatory authority report number is GB-MHRA-WEBCOVID-202107011214257970-CARNQ, Safety Report Unique Identifier GB-MHRA-ADR 25576009. A 35-year-old female patient received first dose bnt162b2 (BNT162B2, Formulation: solution for injection, Batch/Lot Number and Expiration date was not reported), via an unspecified route of administration on an unspecified date as Dose 1, Single for covid-19 immunization. The patient also received second dose bnt162b2 (BNT162B2, Formulation: solution for injection, Batch/Lot Number and Expiration date was not reported), via an unspecified route of administration on 17Mar2021 as Dose 2, Single for covid-19 immunization. Nil significant medical history. Patient has not had symptoms associated with COVID-19. Not had a COVID-19 test. Patient was not enrolled in clinical trial. Patient was not currently breastfeeding. Medical history included miscarriage, pregnancy from 2014 (Details of previous pregnancies: 2014 Live Female), pregnancy from 2017 (Details of previous pregnancies: 2017 Live male), pregnancy (Patient no longer pregnant at the time of reporting), folic acid supplementation. Concomitant medication(s) included folic acid (FOLIC ACID) taken for vitamin supplementation. The patient previously took infanrix ipv hib. On 13Mar2021 the patient experienced miscarriage, on an unspecified date experienced maternal exposure during pregnancy. The patient underwent lab tests and procedures which included ultrasound scan: missed miscarriage on Missed miscarriage at 11weeks (7week size on USS). The outcome of event miscarriage was recovered and for event was unknown. Additional Information: 2 miscarriages following covid vaccine, had 2 successful pregnancies 2014&2017 & never had a miscarriage until after receiving the vaccines. Subsequently had 2 within 4 months. Patient has not tested positive for COVID-19 since having the vaccine. Details of previous pregnancies: 2014 Live Female, 2017 Live male, March 2021 7week miscarriage. Patient was exposed to the medicine Before pregnancy. Details of scans or investigations: Missed miscarriage at 11weeks (7week size on USS).


VAERS ID: 1479669 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Foreign  
Vaccinated:2020-12-23
Onset:2021-03-13
   Days after vaccination:80
Submitted: 0000-00-00
Entered: 2021-07-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Inappropriate schedule of product administration
SMQs:, Termination of pregnancy and risk of abortion (narrow), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021844057

Write-up: Misscarriage; Dosage text: Dose 1, Date and time of start of drug: 23Dec2020; Dosage text: Dose 2, Date and time of start of drug: 17Mar2021.; Misscarriage; This is a spontaneous report from a contactable other health care professional. A 34-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Right on 23Dec2020 (Lot number was not reported) as DOSE 1, SINGLE, dose 2 via an unspecified route of administration, administered in Arm Left on 17Mar2021 (Lot number was not reported) as DOSE 2, SINGLE for COVID-19 immunisation. Medical history included none. There were no concomitant medications. On 13Mar2021, the patient experienced Misscarriage and did not receive treatment and was recovered. On 24Jun2021, the patient experienced Misscarriage and received treatment, and now recovering. Therapeutic measures were taken as a result of misscarriage and included treatment with Medical management of miscarriage. Facility where the most recent COVID-19 vaccine was administered:Workplace clinic. Did the patient receive any other vaccines within 4 weeks prior to the COVID vaccine:No. The adverse event resulted in doctor or other healthcare professional office/clinic visit, and Emergency room/department or urgent care. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient has not been tested for COVID-19.; Sender''s Comments: Based on the limited information provided by the reporter, it appears unlikely that the study drug contributed to the reported events, due to lack of plausible temporal relationship. The case will be reassessed when additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.


VAERS ID: 1706321 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-23
Onset:2021-03-13
   Days after vaccination:18
Submitted: 0000-00-00
Entered: 2021-09-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EP2163 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: SEPFIZER INC202101150210

Write-up: Miscarriage of pregnancy; This is a spontaneous report from a contactable consumer downloaded from the regulatory authority-WEB. This is a report received from Regulatory authority report number SE-MPA-2021-029275 with Safety Report Unique Identifier SE-MPA-2021-029275. A 24-years-old female patient received bnt162b2 (COMIRNATY), dose 2 via an unspecified route of administration on 23Feb2021 (Batch/Lot Number: EP2163) as single dose for covid-19 immunisation . The patient medical history and concomitant medications were not reported. The patient experienced miscarriage of pregnancy (medically significant) on 13Mar2021 with outcome of recovered. The mother reported she became pregnant while taking bnt162b2. The mother was 7 Weeks pregnant at the onset of the event. The mother was pregnant with 1 baby. Course of the event: The woman was vaccinated with dose two on 23Feb2021. Two days later she found out that she was pregnant. On 11Mar2021 she began to have brownish discharge which turned into bleeding two days later. The same day she had excessive bleeding and stomach pain. After examination in hospital, she had a miscarriage. The mother recovered without lasting harm. The case is assessed as serious, important medical event by the Medical Product Agency. No follow-up attempts are possible. No further information expected.


VAERS ID: 1117494 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-03-14
Onset:2021-03-14
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1805018 / 1 RA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Chills, Fatigue, Haemoglobin normal, Headache, Human chorionic gonadotropin normal, Influenza like illness, Myalgia, Pyrexia, Sleep disorder, Ultrasound antenatal screen abnormal, Vaginal haemorrhage
SMQs:, Rhabdomyolysis/myopathy (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Eosinophilic pneumonia (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Megafood Baby & Me 2 Prenatal multivitamin, Nordic Naturals Prenatal DHA Supplement, NatureMade Vitamin D3 supplement
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: IVP Contrast Dye (Iodine)
Diagnostic Lab Data: Blood test to determine hCG hormone levels conducted at facility, 3/16/21 at 4 PM Transvaginal ultrasound conducted at facility, 3/18/21 at 8 AM
CDC Split Type:

Write-up: I started experiencing flu-like symptoms at around 5 PM on 3/14/21. I was feverish and had chills, muscle aches, and a headache. I had very strong chills for a few hours and then I noticed that my resting heart rate was around 128 bpm at around 1:30 AM on 3/15/21. I was running a 100.6 fever at that time. My fever subsided in the morning and the headache persisted throughout the day, and I was very tired as I did not get much sleep the night before. I did not work that day (Monday, 3/15). At the time I was about 7 weeks pregnant. I noticed some very light spotting later in the day on 3/15, and then I continued spotting on 3/16. I consulted a midwife at the facility at 4 PM on 3/16/21 and took a blood test to measure my hCG hormone levels. The following day, 3/17, I received the results that I had a normal level of hCG hormone and normal hemoglobin levels. As the day continued, the spotting turned into bleeding, and eventually the bleeding became heavy starting around 4 PM. I received an ultrasound on 3/18/21 at 8 AM and later spoke with a midwife from facility at 11 AM that day, confirming that there was no viable pregnancy detected via ultrasound. I had lost quite a bit of blood at that point. I am, as of 8:35 PM on Friday, March 19th, still bleeding and experiencing the impact of miscarriage.


VAERS ID: 1171745 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-02-24
Onset:2021-03-14
   Days after vaccination:18
Submitted: 0000-00-00
Entered: 2021-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Ultrasound scan
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins, albuterol inhaler, Symbicort inhaler, pepcid, loratidine.
Current Illness: I was pregnant
Preexisting Conditions: Asthma
Allergies: Dush allergy
Diagnostic Lab Data: An ultrasound exam confirmed the miscarriage on March 15, 2021.
CDC Split Type:

Write-up: I had a miscarriage (spontaneous abortion) on March 14, 2021. I was 12 weeks pregnant at the time of miscarriage.


VAERS ID: 1286967 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-30
Onset:2021-03-14
   Days after vaccination:43
Submitted: 0000-00-00
Entered: 2021-05-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK9788 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: DKPFIZER INC2021430020

Write-up: spontaneous abortion; This is a spontaneous report received from a contactable consumer downloaded from the Regulatory Authority-WEB. The regulatory authority report number is DK-DKMA-WBS-0061058 and DK-DKMA-ADR 25057926. This is the maternal case. A 28-years-old female patient received second dose of bnt162b2 (COMIRNATY, Batch/Lot Number: EK9788; Expiration Date: 31May2021), via an unspecified route of administration on 30Jan2021 as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient previously took first dose of bnt162b2 (COMIRNATY, Batch number: EM0477) for COVID-19 immunization on 09Jan2021. On 14Mar2021, the patient experienced Spontaneous abortion. As a consequence the patient has a medical abortion. The ADR were by the reporter as resulting in hospitalisation. There is no information regarding test results. The patient has not reported any other health issues. The outcome of the event was not recovered. No follow-up attempts are possible. No further information expected.


VAERS ID: 1115752 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Connecticut  
Vaccinated:2021-02-06
Onset:2021-03-15
   Days after vaccination:37
Submitted: 0000-00-00
Entered: 2021-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 004M20A / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Blood test abnormal, Exposure during pregnancy, Human chorionic gonadotropin decreased, Pregnancy test positive, Vaginal haemorrhage
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: omeprazole, prenatal vitamin, zyrtec
Current Illness:
Preexisting Conditions:
Allergies: penicillin
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pregnancy occurred within the 8 days following the vaccine. Pregnancy confirmed with positive urine pregnancy test on 03/01/2021. Some vaginal bleeding began 03/12/2021 but resolved quickly. Abdominal cramping and bleeding on 03/15/2021 and 03/16/2021. Blood work completed on 03/15/2021 and 03/17/2021 showed a decrease in pregnancy hormone and pregnancy was considered miscarried.


VAERS ID: 1141764 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Georgia  
Vaccinated:2021-01-01
Onset:2021-03-15
   Days after vaccination:73
Submitted: 0000-00-00
Entered: 2021-03-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / SYR

Administered by: Military       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Miscarriage
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage


VAERS ID: 1143591 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-03-06
Onset:2021-03-15
   Days after vaccination:9
Submitted: 0000-00-00
Entered: 2021-03-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6199 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EP6955 / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Exposure during pregnancy, Haemorrhage, Ultrasound scan, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: Began spotting/bleeding on 3/15/21 through 3/23/21 and experienced very early miscarriage approximately ~4-5 weeks on/around 3/22/21. Completed blood work and ultrasounds on 3/23/21.
CDC Split Type:

Write-up: ~2 weeks pregnant during time of vaccination,


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https://medalerts.org/vaersdb/findfield.php?EVENTS=ON&PAGENO=7&PERPAGE=100&ESORT=ONSET-DATE&SYMPTOMS[]=Aborted_pregnancy_%2810000209%29&SYMPTOMS[]=Abortion_%2810000210%29&SYMPTOMS[]=Abortion_complete_%2810061614%29&SYMPTOMS[]=Abortion_early_%2810052846%29&SYMPTOMS[]=Abortion_incomplete_%2810000217%29&SYMPTOMS[]=Abortion_induced_%2810000220%29&SYMPTOMS[]=Abortion_late_%2810052847%29&SYMPTOMS[]=Abortion_missed_%2810000230%29&SYMPTOMS[]=Abortion_of_ectopic_pregnancy_%2810066266%29&SYMPTOMS[]=Abortion_spontaneous_%2810000234%29&SYMPTOMS[]=Abortion_spontaneous_complete_%2810061616%29&SYMPTOMS[]=Abortion_spontaneous_incomplete_%2810061617%29&SYMPTOMS[]=Foetal_cardiac_arrest_%2810084280%29&SYMPTOMS[]=Foetal_death_%2810055690%29&SYMPTOMS[]=Premature_baby_death_%2810076700%29&SYMPTOMS[]=Premature_delivery_%2810036595%29&SYMPTOMS[]=Stillbirth_%2810042062%29&VAX=COVID19


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